G309D and W437OPA PINK1 mutations in Caucasian Parkinson's disease patients
Identifieur interne : 001153 ( Main/Merge ); précédent : 001152; suivant : 001154G309D and W437OPA PINK1 mutations in Caucasian Parkinson's disease patients
Auteurs : H Deng [États-Unis] ; W Le [États-Unis] ; X Zhang [États-Unis] ; T Pan [États-Unis] ; J Jankovic [États-Unis]Source :
- Acta Neurologica Scandinavica [ 0001-6314 ] ; 2005-06.
Descripteurs français
- Wicri :
- geographic : États-Unis.
English descriptors
- KwdEn :
- Adult, Amino Acid Substitution, Caucasian, DNA Mutational Analysis, European Continental Ancestry Group (genetics), Female, G309D, Genetic Testing, Genome, Human, Humans, Male, Middle Aged, Mutation (genetics), PINK1, Parkinson Disease (ethnology), Parkinson Disease (genetics), Parkinson Disease (metabolism), Parkinson's disease, Protein Kinases (genetics), United States, W437OPA.
- MESH :
- chemical , genetics : Protein Kinases.
- geographic : United States.
- ethnology : Parkinson Disease.
- genetics : European Continental Ancestry Group, Mutation, Parkinson Disease.
- metabolism : Parkinson Disease.
- Adult, Amino Acid Substitution, DNA Mutational Analysis, Female, Genetic Testing, Genome, Human, Humans, Male, Middle Aged.
Abstract
Objective – To determine whether the G309D and W437OPA mutations in PINK1 gene are present in American Caucasian population of patients with Parkinson's disease (PD). Methods – We searched for the G309D and W437OPA mutation by sequencing the regions of interest in the PINK1 gene in 237 unrelated Caucasian patients. Results – None of the 237 samples showed the G309D or W437OPA mutations. Conclusions – The G309D and W437OPA mutations in PINK1 gene probably do not represent common causes of familial or sporadic PD in a Caucasian population.
Url:
DOI: 10.1111/j.1600-0404.2005.00383.x
Links toward previous steps (curation, corpus...)
- to stream Istex, to step Corpus: 000E04
- to stream Istex, to step Curation: 000E04
- to stream Istex, to step Checkpoint: 000D06
- to stream PubMed, to step Corpus: 000198
- to stream PubMed, to step Curation: 000198
- to stream PubMed, to step Checkpoint: 000196
- to stream Ncbi, to step Merge: 000091
- to stream Ncbi, to step Curation: 000091
- to stream Ncbi, to step Checkpoint: 000091
Links to Exploration step
ISTEX:7454C0DB6D7A9A8C21D4D4C54E1484E8BA4B5342Le document en format XML
<record><TEI wicri:istexFullTextTei="biblStruct"><teiHeader><fileDesc><titleStmt><title xml:lang="en">G309D and W437OPA PINK1 mutations in Caucasian Parkinson's disease patients</title>
<author><name sortKey="Deng, H" sort="Deng, H" uniqKey="Deng H" first="H" last="Deng">H Deng</name>
</author>
<author><name sortKey="Le, W D" sort="Le, W D" uniqKey="Le W" first="W" last="Le">W Le</name>
</author>
<author><name sortKey="Zhang, X" sort="Zhang, X" uniqKey="Zhang X" first="X" last="Zhang">X Zhang</name>
</author>
<author><name sortKey="Pan, T H" sort="Pan, T H" uniqKey="Pan T" first="T" last="Pan">T Pan</name>
</author>
<author><name sortKey="Jankovic, J" sort="Jankovic, J" uniqKey="Jankovic J" first="J" last="Jankovic">J Jankovic</name>
</author>
</titleStmt>
<publicationStmt><idno type="wicri:source">ISTEX</idno>
<idno type="RBID">ISTEX:7454C0DB6D7A9A8C21D4D4C54E1484E8BA4B5342</idno>
<date when="2005" year="2005">2005</date>
<idno type="doi">10.1111/j.1600-0404.2005.00383.x</idno>
<idno type="url">https://api.istex.fr/document/7454C0DB6D7A9A8C21D4D4C54E1484E8BA4B5342/fulltext/pdf</idno>
<idno type="wicri:Area/Istex/Corpus">000E04</idno>
<idno type="wicri:Area/Istex/Curation">000E04</idno>
<idno type="wicri:Area/Istex/Checkpoint">000D06</idno>
<idno type="wicri:doubleKey">0001-6314:2005:Deng H:g:d:and</idno>
<idno type="wicri:source">PubMed</idno>
<idno type="RBID">pubmed:15876334</idno>
<idno type="wicri:Area/PubMed/Corpus">000198</idno>
<idno type="wicri:Area/PubMed/Curation">000198</idno>
<idno type="wicri:Area/PubMed/Checkpoint">000196</idno>
<idno type="wicri:Area/Ncbi/Merge">000091</idno>
<idno type="wicri:Area/Ncbi/Curation">000091</idno>
<idno type="wicri:Area/Ncbi/Checkpoint">000091</idno>
<idno type="wicri:doubleKey">0001-6314:2005:Deng H:g:d:and</idno>
<idno type="wicri:Area/Main/Merge">001153</idno>
</publicationStmt>
<sourceDesc><biblStruct><analytic><title level="a" type="main" xml:lang="en">G309D and W437OPA PINK1 mutations in Caucasian Parkinson's disease patients</title>
<author><name sortKey="Deng, H" sort="Deng, H" uniqKey="Deng H" first="H" last="Deng">H Deng</name>
<affiliation wicri:level="2"><country xml:lang="fr">États-Unis</country>
<wicri:regionArea>Department of Neurology, Parkinson's Disease Center and Movement Disorders Clinic, Baylor College of Medicine, Houston, TX</wicri:regionArea>
<placeName><region type="state">Texas</region>
</placeName>
</affiliation>
</author>
<author><name sortKey="Le, W D" sort="Le, W D" uniqKey="Le W" first="W" last="Le">W Le</name>
<affiliation wicri:level="2"><country xml:lang="fr">États-Unis</country>
<wicri:regionArea>Department of Neurology, Parkinson's Disease Center and Movement Disorders Clinic, Baylor College of Medicine, Houston, TX</wicri:regionArea>
<placeName><region type="state">Texas</region>
</placeName>
</affiliation>
</author>
<author><name sortKey="Zhang, X" sort="Zhang, X" uniqKey="Zhang X" first="X" last="Zhang">X Zhang</name>
<affiliation wicri:level="2"><country xml:lang="fr">États-Unis</country>
<wicri:regionArea>Department of Neurology, Parkinson's Disease Center and Movement Disorders Clinic, Baylor College of Medicine, Houston, TX</wicri:regionArea>
<placeName><region type="state">Texas</region>
</placeName>
</affiliation>
</author>
<author><name sortKey="Pan, T H" sort="Pan, T H" uniqKey="Pan T" first="T" last="Pan">T Pan</name>
<affiliation wicri:level="2"><country xml:lang="fr">États-Unis</country>
<wicri:regionArea>Department of Neurology, Parkinson's Disease Center and Movement Disorders Clinic, Baylor College of Medicine, Houston, TX</wicri:regionArea>
<placeName><region type="state">Texas</region>
</placeName>
</affiliation>
</author>
<author><name sortKey="Jankovic, J" sort="Jankovic, J" uniqKey="Jankovic J" first="J" last="Jankovic">J Jankovic</name>
<affiliation wicri:level="2"><country xml:lang="fr">États-Unis</country>
<wicri:regionArea>Department of Neurology, Parkinson's Disease Center and Movement Disorders Clinic, Baylor College of Medicine, Houston, TX</wicri:regionArea>
<placeName><region type="state">Texas</region>
</placeName>
</affiliation>
</author>
</analytic>
<monogr></monogr>
<series><title level="j">Acta Neurologica Scandinavica</title>
<idno type="ISSN">0001-6314</idno>
<idno type="eISSN">1600-0404</idno>
<imprint><publisher>Munksgaard International Publishers</publisher>
<pubPlace>Oxford, UK</pubPlace>
<date type="published" when="2005-06">2005-06</date>
<biblScope unit="volume">111</biblScope>
<biblScope unit="issue">6</biblScope>
<biblScope unit="page" from="351">351</biblScope>
<biblScope unit="page" to="352">352</biblScope>
</imprint>
<idno type="ISSN">0001-6314</idno>
</series>
<idno type="istex">7454C0DB6D7A9A8C21D4D4C54E1484E8BA4B5342</idno>
<idno type="DOI">10.1111/j.1600-0404.2005.00383.x</idno>
<idno type="ArticleID">ANE383</idno>
</biblStruct>
</sourceDesc>
<seriesStmt><idno type="ISSN">0001-6314</idno>
</seriesStmt>
</fileDesc>
<profileDesc><textClass><keywords scheme="KwdEn" xml:lang="en"><term>Adult</term>
<term>Amino Acid Substitution</term>
<term>Caucasian</term>
<term>DNA Mutational Analysis</term>
<term>European Continental Ancestry Group (genetics)</term>
<term>Female</term>
<term>G309D</term>
<term>Genetic Testing</term>
<term>Genome, Human</term>
<term>Humans</term>
<term>Male</term>
<term>Middle Aged</term>
<term>Mutation (genetics)</term>
<term>PINK1</term>
<term>Parkinson Disease (ethnology)</term>
<term>Parkinson Disease (genetics)</term>
<term>Parkinson Disease (metabolism)</term>
<term>Parkinson's disease</term>
<term>Protein Kinases (genetics)</term>
<term>United States</term>
<term>W437OPA</term>
</keywords>
<keywords scheme="MESH" type="chemical" qualifier="genetics" xml:lang="en"><term>Protein Kinases</term>
</keywords>
<keywords scheme="MESH" type="geographic" xml:lang="en"><term>United States</term>
</keywords>
<keywords scheme="MESH" qualifier="ethnology" xml:lang="en"><term>Parkinson Disease</term>
</keywords>
<keywords scheme="MESH" qualifier="genetics" xml:lang="en"><term>European Continental Ancestry Group</term>
<term>Mutation</term>
<term>Parkinson Disease</term>
</keywords>
<keywords scheme="MESH" qualifier="metabolism" xml:lang="en"><term>Parkinson Disease</term>
</keywords>
<keywords scheme="MESH" xml:lang="en"><term>Adult</term>
<term>Amino Acid Substitution</term>
<term>DNA Mutational Analysis</term>
<term>Female</term>
<term>Genetic Testing</term>
<term>Genome, Human</term>
<term>Humans</term>
<term>Male</term>
<term>Middle Aged</term>
</keywords>
<keywords scheme="Wicri" type="geographic" xml:lang="fr"><term>États-Unis</term>
</keywords>
</textClass>
<langUsage><language ident="en">en</language>
</langUsage>
</profileDesc>
</teiHeader>
<front><div type="abstract" xml:lang="en">Objective – To determine whether the G309D and W437OPA mutations in PINK1 gene are present in American Caucasian population of patients with Parkinson's disease (PD). Methods – We searched for the G309D and W437OPA mutation by sequencing the regions of interest in the PINK1 gene in 237 unrelated Caucasian patients. Results – None of the 237 samples showed the G309D or W437OPA mutations. Conclusions – The G309D and W437OPA mutations in PINK1 gene probably do not represent common causes of familial or sporadic PD in a Caucasian population.</div>
</front>
</TEI>
<double doi="10.1111/j.1600-0404.2005.00383.x"><ISTEX><TEI wicri:istexFullTextTei="biblStruct"><teiHeader><fileDesc><titleStmt><title xml:lang="en">G309D and W437OPA PINK1 mutations in Caucasian Parkinson's disease patients</title>
<author><name sortKey="Deng, H" sort="Deng, H" uniqKey="Deng H" first="H" last="Deng">H Deng</name>
</author>
<author><name sortKey="Le, W D" sort="Le, W D" uniqKey="Le W" first="W" last="Le">W Le</name>
</author>
<author><name sortKey="Zhang, X" sort="Zhang, X" uniqKey="Zhang X" first="X" last="Zhang">X Zhang</name>
</author>
<author><name sortKey="Pan, T H" sort="Pan, T H" uniqKey="Pan T" first="T" last="Pan">T Pan</name>
</author>
<author><name sortKey="Jankovic, J" sort="Jankovic, J" uniqKey="Jankovic J" first="J" last="Jankovic">J Jankovic</name>
</author>
</titleStmt>
<publicationStmt><idno type="wicri:source">ISTEX</idno>
<idno type="RBID">ISTEX:7454C0DB6D7A9A8C21D4D4C54E1484E8BA4B5342</idno>
<date when="2005" year="2005">2005</date>
<idno type="doi">10.1111/j.1600-0404.2005.00383.x</idno>
<idno type="url">https://api.istex.fr/document/7454C0DB6D7A9A8C21D4D4C54E1484E8BA4B5342/fulltext/pdf</idno>
<idno type="wicri:Area/Istex/Corpus">000E04</idno>
<idno type="wicri:Area/Istex/Curation">000E04</idno>
<idno type="wicri:Area/Istex/Checkpoint">000D06</idno>
<idno type="wicri:doubleKey">0001-6314:2005:Deng H:g:d:and</idno>
</publicationStmt>
<sourceDesc><biblStruct><analytic><title level="a" type="main" xml:lang="en">G309D and W437OPA PINK1 mutations in Caucasian Parkinson's disease patients</title>
<author><name sortKey="Deng, H" sort="Deng, H" uniqKey="Deng H" first="H" last="Deng">H Deng</name>
<affiliation wicri:level="2"><country xml:lang="fr">États-Unis</country>
<wicri:regionArea>Department of Neurology, Parkinson's Disease Center and Movement Disorders Clinic, Baylor College of Medicine, Houston, TX</wicri:regionArea>
<placeName><region type="state">Texas</region>
</placeName>
</affiliation>
</author>
<author><name sortKey="Le, W D" sort="Le, W D" uniqKey="Le W" first="W" last="Le">W Le</name>
<affiliation wicri:level="2"><country xml:lang="fr">États-Unis</country>
<wicri:regionArea>Department of Neurology, Parkinson's Disease Center and Movement Disorders Clinic, Baylor College of Medicine, Houston, TX</wicri:regionArea>
<placeName><region type="state">Texas</region>
</placeName>
</affiliation>
</author>
<author><name sortKey="Zhang, X" sort="Zhang, X" uniqKey="Zhang X" first="X" last="Zhang">X Zhang</name>
<affiliation wicri:level="2"><country xml:lang="fr">États-Unis</country>
<wicri:regionArea>Department of Neurology, Parkinson's Disease Center and Movement Disorders Clinic, Baylor College of Medicine, Houston, TX</wicri:regionArea>
<placeName><region type="state">Texas</region>
</placeName>
</affiliation>
</author>
<author><name sortKey="Pan, T H" sort="Pan, T H" uniqKey="Pan T" first="T" last="Pan">T Pan</name>
<affiliation wicri:level="2"><country xml:lang="fr">États-Unis</country>
<wicri:regionArea>Department of Neurology, Parkinson's Disease Center and Movement Disorders Clinic, Baylor College of Medicine, Houston, TX</wicri:regionArea>
<placeName><region type="state">Texas</region>
</placeName>
</affiliation>
</author>
<author><name sortKey="Jankovic, J" sort="Jankovic, J" uniqKey="Jankovic J" first="J" last="Jankovic">J Jankovic</name>
<affiliation wicri:level="2"><country xml:lang="fr">États-Unis</country>
<wicri:regionArea>Department of Neurology, Parkinson's Disease Center and Movement Disorders Clinic, Baylor College of Medicine, Houston, TX</wicri:regionArea>
<placeName><region type="state">Texas</region>
</placeName>
</affiliation>
</author>
</analytic>
<monogr></monogr>
<series><title level="j">Acta Neurologica Scandinavica</title>
<idno type="ISSN">0001-6314</idno>
<idno type="eISSN">1600-0404</idno>
<imprint><publisher>Munksgaard International Publishers</publisher>
<pubPlace>Oxford, UK</pubPlace>
<date type="published" when="2005-06">2005-06</date>
<biblScope unit="volume">111</biblScope>
<biblScope unit="issue">6</biblScope>
<biblScope unit="page" from="351">351</biblScope>
<biblScope unit="page" to="352">352</biblScope>
</imprint>
<idno type="ISSN">0001-6314</idno>
</series>
<idno type="istex">7454C0DB6D7A9A8C21D4D4C54E1484E8BA4B5342</idno>
<idno type="DOI">10.1111/j.1600-0404.2005.00383.x</idno>
<idno type="ArticleID">ANE383</idno>
</biblStruct>
</sourceDesc>
<seriesStmt><idno type="ISSN">0001-6314</idno>
</seriesStmt>
</fileDesc>
<profileDesc><textClass><keywords scheme="KwdEn" xml:lang="en"><term>Caucasian</term>
<term>G309D</term>
<term>PINK1</term>
<term>Parkinson's disease</term>
<term>W437OPA</term>
</keywords>
</textClass>
<langUsage><language ident="en">en</language>
</langUsage>
</profileDesc>
</teiHeader>
<front><div type="abstract" xml:lang="en">Objective – To determine whether the G309D and W437OPA mutations in PINK1 gene are present in American Caucasian population of patients with Parkinson's disease (PD). Methods – We searched for the G309D and W437OPA mutation by sequencing the regions of interest in the PINK1 gene in 237 unrelated Caucasian patients. Results – None of the 237 samples showed the G309D or W437OPA mutations. Conclusions – The G309D and W437OPA mutations in PINK1 gene probably do not represent common causes of familial or sporadic PD in a Caucasian population.</div>
</front>
</TEI>
</ISTEX>
<PubMed><TEI><teiHeader><fileDesc><titleStmt><title xml:lang="en">G309D and W437OPA PINK1 mutations in Caucasian Parkinson's disease patients.</title>
<author><name sortKey="Deng, H" sort="Deng, H" uniqKey="Deng H" first="H" last="Deng">H. Deng</name>
<affiliation wicri:level="2"><nlm:affiliation>Department of Neurology, Parkinson's Disease Center and Movement Disorders Clinic, Baylor College of Medicine, Houston, TX 77030, USA.</nlm:affiliation>
<country xml:lang="fr">États-Unis</country>
<wicri:regionArea>Department of Neurology, Parkinson's Disease Center and Movement Disorders Clinic, Baylor College of Medicine, Houston, TX 77030</wicri:regionArea>
<placeName><region type="state">Texas</region>
</placeName>
</affiliation>
</author>
<author><name sortKey="Le, W D" sort="Le, W D" uniqKey="Le W" first="W" last="Le">W Le</name>
</author>
<author><name sortKey="Zhang, X" sort="Zhang, X" uniqKey="Zhang X" first="X" last="Zhang">X. Zhang</name>
</author>
<author><name sortKey="Pan, T H" sort="Pan, T H" uniqKey="Pan T" first="T" last="Pan">T Pan</name>
</author>
<author><name sortKey="Jankovic, J" sort="Jankovic, J" uniqKey="Jankovic J" first="J" last="Jankovic">Joseph Jankovic</name>
<affiliation><country>États-Unis</country>
<placeName><settlement type="city">Houston</settlement>
<region type="state">Texas</region>
</placeName>
<orgName type="university" n="3">Baylor College of Medicine</orgName>
</affiliation>
</author>
</titleStmt>
<publicationStmt><idno type="wicri:source">PubMed</idno>
<date when="2005">2005</date>
<idno type="doi">10.1111/j.1600-0404.2005.00383.x</idno>
<idno type="RBID">pubmed:15876334</idno>
<idno type="pmid">15876334</idno>
<idno type="wicri:Area/PubMed/Corpus">000198</idno>
<idno type="wicri:Area/PubMed/Curation">000198</idno>
<idno type="wicri:Area/PubMed/Checkpoint">000196</idno>
<idno type="wicri:Area/Ncbi/Merge">000091</idno>
<idno type="wicri:Area/Ncbi/Curation">000091</idno>
<idno type="wicri:Area/Ncbi/Checkpoint">000091</idno>
<idno type="wicri:doubleKey">0001-6314:2005:Deng H:g:d:and</idno>
</publicationStmt>
<sourceDesc><biblStruct><analytic><title xml:lang="en">G309D and W437OPA PINK1 mutations in Caucasian Parkinson's disease patients.</title>
<author><name sortKey="Deng, H" sort="Deng, H" uniqKey="Deng H" first="H" last="Deng">H. Deng</name>
<affiliation wicri:level="2"><nlm:affiliation>Department of Neurology, Parkinson's Disease Center and Movement Disorders Clinic, Baylor College of Medicine, Houston, TX 77030, USA.</nlm:affiliation>
<country xml:lang="fr">États-Unis</country>
<wicri:regionArea>Department of Neurology, Parkinson's Disease Center and Movement Disorders Clinic, Baylor College of Medicine, Houston, TX 77030</wicri:regionArea>
<placeName><region type="state">Texas</region>
</placeName>
</affiliation>
</author>
<author><name sortKey="Le, W D" sort="Le, W D" uniqKey="Le W" first="W" last="Le">W Le</name>
</author>
<author><name sortKey="Zhang, X" sort="Zhang, X" uniqKey="Zhang X" first="X" last="Zhang">X. Zhang</name>
</author>
<author><name sortKey="Pan, T H" sort="Pan, T H" uniqKey="Pan T" first="T" last="Pan">T Pan</name>
</author>
<author><name sortKey="Jankovic, J" sort="Jankovic, J" uniqKey="Jankovic J" first="J" last="Jankovic">Joseph Jankovic</name>
<affiliation><country>États-Unis</country>
<placeName><settlement type="city">Houston</settlement>
<region type="state">Texas</region>
</placeName>
<orgName type="university" n="3">Baylor College of Medicine</orgName>
</affiliation>
</author>
</analytic>
<series><title level="j">Acta neurologica Scandinavica</title>
<idno type="ISSN">0001-6314</idno>
<imprint><date when="2005" type="published">2005</date>
</imprint>
</series>
</biblStruct>
</sourceDesc>
</fileDesc>
<profileDesc><textClass><keywords scheme="KwdEn" xml:lang="en"><term>Adult</term>
<term>Amino Acid Substitution</term>
<term>DNA Mutational Analysis</term>
<term>European Continental Ancestry Group (genetics)</term>
<term>Female</term>
<term>Genetic Testing</term>
<term>Genome, Human</term>
<term>Humans</term>
<term>Male</term>
<term>Middle Aged</term>
<term>Mutation (genetics)</term>
<term>Parkinson Disease (ethnology)</term>
<term>Parkinson Disease (genetics)</term>
<term>Parkinson Disease (metabolism)</term>
<term>Protein Kinases (genetics)</term>
<term>United States</term>
</keywords>
<keywords scheme="MESH" type="chemical" qualifier="genetics" xml:lang="en"><term>Protein Kinases</term>
</keywords>
<keywords scheme="MESH" type="geographic" xml:lang="en"><term>United States</term>
</keywords>
<keywords scheme="MESH" qualifier="ethnology" xml:lang="en"><term>Parkinson Disease</term>
</keywords>
<keywords scheme="MESH" qualifier="genetics" xml:lang="en"><term>European Continental Ancestry Group</term>
<term>Mutation</term>
<term>Parkinson Disease</term>
</keywords>
<keywords scheme="MESH" qualifier="metabolism" xml:lang="en"><term>Parkinson Disease</term>
</keywords>
<keywords scheme="MESH" xml:lang="en"><term>Adult</term>
<term>Amino Acid Substitution</term>
<term>DNA Mutational Analysis</term>
<term>Female</term>
<term>Genetic Testing</term>
<term>Genome, Human</term>
<term>Humans</term>
<term>Male</term>
<term>Middle Aged</term>
</keywords>
<keywords scheme="Wicri" type="geographic" xml:lang="fr"><term>États-Unis</term>
</keywords>
</textClass>
</profileDesc>
</teiHeader>
<front><div type="abstract" xml:lang="en">To determine whether the G309D and W437OPA mutations in PINK1 gene are present in American Caucasian population of patients with Parkinson's disease (PD).</div>
</front>
</TEI>
</PubMed>
</double>
</record>
Pour manipuler ce document sous Unix (Dilib)
EXPLOR_STEP=$WICRI_ROOT/Wicri/Santé/explor/JankovicV1/Data/Main/Merge
HfdSelect -h $EXPLOR_STEP/biblio.hfd -nk 001153 | SxmlIndent | more
Ou
HfdSelect -h $EXPLOR_AREA/Data/Main/Merge/biblio.hfd -nk 001153 | SxmlIndent | more
Pour mettre un lien sur cette page dans le réseau Wicri
{{Explor lien |wiki= Wicri/Santé |area= JankovicV1 |flux= Main |étape= Merge |type= RBID |clé= ISTEX:7454C0DB6D7A9A8C21D4D4C54E1484E8BA4B5342 |texte= G309D and W437OPA PINK1 mutations in Caucasian Parkinson's disease patients }}
![]() | This area was generated with Dilib version V0.6.19. | ![]() |