G309D and W4370PA PINK1 mutations in Caucasian Parkinson's disease patients
Identifieur interne : 001206 ( Main/Merge ); précédent : 001205; suivant : 001207G309D and W4370PA 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.
Descripteurs français
- Pascal (Inist)
- Wicri :
- topic : Homme.
English descriptors
- KwdEn :
Abstract
Objective - To determine whether the G309D and W4370PA mutations in PINK1 gene are present in American Caucasian population of patients with Parkinson's disease (PD). Methods - We searched for the G309D and W4370PA 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 W4370PA mutations. Conclusions - The G309D and W4370PA mutations in PINK1 gene probably do not represent common causes of familial or sporadic PD in a Caucasian population.
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aut.</sZ><sZ>5 aut.</sZ></inist:fA14><country>États-Unis</country><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"><inist:fA14 i1="01"><s1>Department of Neurology, Parkinson's Disease Center and Movement Disorders Clinic, Baylor College of Medicine</s1><s2>Houston, TX</s2><s3>USA</s3><sZ>1 aut.</sZ><sZ>2 aut.</sZ><sZ>3 aut.</sZ><sZ>4 aut.</sZ><sZ>5 aut.</sZ></inist:fA14><country>États-Unis</country><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"><inist:fA14 i1="01"><s1>Department of Neurology, Parkinson's Disease Center and Movement Disorders Clinic, Baylor College of Medicine</s1><s2>Houston, TX</s2><s3>USA</s3><sZ>1 aut.</sZ><sZ>2 aut.</sZ><sZ>3 aut.</sZ><sZ>4 aut.</sZ><sZ>5 aut.</sZ></inist:fA14><country>États-Unis</country><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"><inist:fA14 i1="01"><s1>Department of Neurology, Parkinson's Disease Center and Movement Disorders Clinic, Baylor College of Medicine</s1><s2>Houston, TX</s2><s3>USA</s3><sZ>1 aut.</sZ><sZ>2 aut.</sZ><sZ>3 aut.</sZ><sZ>4 aut.</sZ><sZ>5 aut.</sZ></inist:fA14><country>États-Unis</country><placeName><region type="state">Texas</region></placeName></affiliation></author></titleStmt><publicationStmt><idno type="wicri:source">INIST</idno><idno type="inist">05-0261960</idno><date when="2005">2005</date><idno type="stanalyst">PASCAL 05-0261960 INIST</idno><idno type="RBID">Pascal:05-0261960</idno><idno type="wicri:Area/PascalFrancis/Corpus">000091</idno><idno type="wicri:Area/PascalFrancis/Curation">000075</idno><idno type="wicri:Area/PascalFrancis/Checkpoint">000086</idno><idno type="wicri:doubleKey">0001-6314:2005:Deng H:g:d:and</idno><idno type="wicri:Area/Main/Merge">001206</idno></publicationStmt><sourceDesc><biblStruct><analytic><title xml:lang="en" level="a">G309D and W4370PA 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"><inist:fA14 i1="01"><s1>Department of Neurology, Parkinson's Disease Center and Movement Disorders Clinic, Baylor College of Medicine</s1><s2>Houston, TX</s2><s3>USA</s3><sZ>1 aut.</sZ><sZ>2 aut.</sZ><sZ>3 aut.</sZ><sZ>4 aut.</sZ><sZ>5 aut.</sZ></inist:fA14><country>États-Unis</country><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"><inist:fA14 i1="01"><s1>Department of Neurology, Parkinson's Disease Center and Movement Disorders Clinic, Baylor College of Medicine</s1><s2>Houston, TX</s2><s3>USA</s3><sZ>1 aut.</sZ><sZ>2 aut.</sZ><sZ>3 aut.</sZ><sZ>4 aut.</sZ><sZ>5 aut.</sZ></inist:fA14><country>États-Unis</country><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"><inist:fA14 i1="01"><s1>Department of Neurology, Parkinson's Disease Center and Movement Disorders Clinic, Baylor College of Medicine</s1><s2>Houston, TX</s2><s3>USA</s3><sZ>1 aut.</sZ><sZ>2 aut.</sZ><sZ>3 aut.</sZ><sZ>4 aut.</sZ><sZ>5 aut.</sZ></inist:fA14><country>États-Unis</country><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"><inist:fA14 i1="01"><s1>Department of Neurology, Parkinson's Disease Center and Movement Disorders Clinic, Baylor College of Medicine</s1><s2>Houston, TX</s2><s3>USA</s3><sZ>1 aut.</sZ><sZ>2 aut.</sZ><sZ>3 aut.</sZ><sZ>4 aut.</sZ><sZ>5 aut.</sZ></inist:fA14><country>États-Unis</country><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"><inist:fA14 i1="01"><s1>Department of Neurology, Parkinson's Disease Center and Movement Disorders Clinic, Baylor College of Medicine</s1><s2>Houston, TX</s2><s3>USA</s3><sZ>1 aut.</sZ><sZ>2 aut.</sZ><sZ>3 aut.</sZ><sZ>4 aut.</sZ><sZ>5 aut.</sZ></inist:fA14><country>États-Unis</country><placeName><region type="state">Texas</region></placeName></affiliation></author></analytic><series><title level="j" type="main">Acta neurologica scandinavica</title><title level="j" type="abbreviated">Acta neurol. scand.</title><idno type="ISSN">0001-6314</idno><imprint><date when="2005">2005</date></imprint></series></biblStruct></sourceDesc><seriesStmt><title level="j" type="main">Acta neurologica scandinavica</title><title level="j" type="abbreviated">Acta neurol. scand.</title><idno type="ISSN">0001-6314</idno></seriesStmt></fileDesc><profileDesc><textClass><keywords scheme="KwdEn" xml:lang="en"><term>Human</term><term>Mutation</term><term>Nervous system diseases</term><term>Parkinson disease</term></keywords><keywords scheme="Pascal" xml:lang="fr"><term>Système nerveux pathologie</term><term>Mutation</term><term>Homme</term><term>Parkinson maladie</term></keywords><keywords scheme="Wicri" type="topic" xml:lang="fr"><term>Homme</term></keywords></textClass></profileDesc></teiHeader><front><div type="abstract" xml:lang="en">Objective - To determine whether the G309D and W4370PA mutations in PINK1 gene are present in American Caucasian population of patients with Parkinson's disease (PD). Methods - We searched for the G309D and W4370PA 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 W4370PA mutations. Conclusions - The G309D and W4370PA mutations in PINK1 gene probably do not represent common causes of familial or sporadic PD in a Caucasian population.</div></front></TEI><affiliations><list><country><li>États-Unis</li></country><region><li>Texas</li></region></list><tree><country name="États-Unis"><region name="Texas"><name sortKey="Deng, H" sort="Deng, H" uniqKey="Deng H" first="H" last="Deng">H Deng</name></region><name sortKey="Jankovic, J" sort="Jankovic, J" uniqKey="Jankovic J" first="J" last="Jankovic">J Jankovic</name><name sortKey="Le, W D" sort="Le, W D" uniqKey="Le W" first="W" last="Le">W Le</name><name sortKey="Pan, T H" sort="Pan, T H" uniqKey="Pan T" first="T" last="Pan">T Pan</name><name sortKey="Zhang, X" sort="Zhang, X" uniqKey="Zhang X" first="X" last="Zhang">X Zhang</name></country></tree></affiliations></record>Pour manipuler ce document sous Unix (Dilib)
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