The G2019S LRRK2 mutation is uncommon amongst Greek patients with sporadic Parkinson's disease
Identifieur interne : 000F41 ( Main/Exploration ); précédent : 000F40; suivant : 000F42The G2019S LRRK2 mutation is uncommon amongst Greek patients with sporadic Parkinson's disease
Auteurs : K. Kalinderi [Grèce] ; L. Fidani [Grèce] ; S. Bostantjopoulou [Grèce] ; Z. Katsarou [Grèce] ; A. Kotsis [Grèce]Source :
- European Journal of Neurology [ 1351-5101 ] ; 2007-10.
English descriptors
Abstract
Parkinson's disease (PD) is the second most common neurodegenerative disorder affecting approximately 2% of the population >60 years of age. Although, the etiology of PD is still unknown, the genetic background of the disease has been documented. Recently, a mutation in the LRRK2 gene, G2019S, was associated with 3–41% and 1–2% of familial and sporadic PD, respectively suggesting a pivotal role of LRRK2 in PD. In this report, we examine the association of the G2019S mutation with sporadic late‐onset PD, in an independent cohort of Greek patients and controls.
Url:
DOI: 10.1111/j.1468-1331.2007.01867.x
Affiliations:
Links toward previous steps (curation, corpus...)
Le document en format XML
<record><TEI wicri:istexFullTextTei="biblStruct"><teiHeader><fileDesc><titleStmt><title xml:lang="en">The G2019S LRRK2 mutation is uncommon amongst Greek patients with sporadic Parkinson's disease</title>
<author><name sortKey="Kalinderi, K" sort="Kalinderi, K" uniqKey="Kalinderi K" first="K." last="Kalinderi">K. Kalinderi</name>
</author>
<author><name sortKey="Fidani, L" sort="Fidani, L" uniqKey="Fidani L" first="L." last="Fidani">L. Fidani</name>
</author>
<author><name sortKey="Bostantjopoulou, S" sort="Bostantjopoulou, S" uniqKey="Bostantjopoulou S" first="S." last="Bostantjopoulou">S. Bostantjopoulou</name>
</author>
<author><name sortKey="Katsarou, Z" sort="Katsarou, Z" uniqKey="Katsarou Z" first="Z." last="Katsarou">Z. Katsarou</name>
</author>
<author><name sortKey="Kotsis, A" sort="Kotsis, A" uniqKey="Kotsis A" first="A." last="Kotsis">A. Kotsis</name>
</author>
</titleStmt>
<publicationStmt><idno type="wicri:source">ISTEX</idno>
<idno type="RBID">ISTEX:0E35C463024562ADDCC87D7F105411C10D63BE6A</idno>
<date when="2007" year="2007">2007</date>
<idno type="doi">10.1111/j.1468-1331.2007.01867.x</idno>
<idno type="url">https://api.istex.fr/document/0E35C463024562ADDCC87D7F105411C10D63BE6A/fulltext/pdf</idno>
<idno type="wicri:Area/Main/Corpus">002F85</idno>
<idno type="wicri:Area/Main/Curation">002B95</idno>
<idno type="wicri:Area/Main/Exploration">000F41</idno>
</publicationStmt>
<sourceDesc><biblStruct><analytic><title level="a" type="main" xml:lang="en">The G2019S LRRK2 mutation is uncommon amongst Greek patients with sporadic Parkinson's disease</title>
<author><name sortKey="Kalinderi, K" sort="Kalinderi, K" uniqKey="Kalinderi K" first="K." last="Kalinderi">K. Kalinderi</name>
<affiliation wicri:level="1"><country xml:lang="fr">Grèce</country>
<wicri:regionArea>Department of General Biology, Medical School, Aristotle University of Thessaloniki, Thessaloniki</wicri:regionArea>
<wicri:noRegion>Thessaloniki</wicri:noRegion>
</affiliation>
</author>
<author><name sortKey="Fidani, L" sort="Fidani, L" uniqKey="Fidani L" first="L." last="Fidani">L. Fidani</name>
<affiliation wicri:level="1"><country xml:lang="fr">Grèce</country>
<wicri:regionArea>Department of General Biology, Medical School, Aristotle University of Thessaloniki, Thessaloniki</wicri:regionArea>
<wicri:noRegion>Thessaloniki</wicri:noRegion>
</affiliation>
</author>
<author><name sortKey="Bostantjopoulou, S" sort="Bostantjopoulou, S" uniqKey="Bostantjopoulou S" first="S." last="Bostantjopoulou">S. Bostantjopoulou</name>
<affiliation wicri:level="1"><country xml:lang="fr">Grèce</country>
<wicri:regionArea>Third Department of Neurology, G. Papanikolaou Hospital, Aristotle University of Thessaloniki, Thessaloniki</wicri:regionArea>
<wicri:noRegion>Thessaloniki</wicri:noRegion>
</affiliation>
</author>
<author><name sortKey="Katsarou, Z" sort="Katsarou, Z" uniqKey="Katsarou Z" first="Z." last="Katsarou">Z. Katsarou</name>
<affiliation wicri:level="1"><country xml:lang="fr">Grèce</country>
<wicri:regionArea>Third Department of Neurology, G. Papanikolaou Hospital, Aristotle University of Thessaloniki, Thessaloniki</wicri:regionArea>
<wicri:noRegion>Thessaloniki</wicri:noRegion>
</affiliation>
</author>
<author><name sortKey="Kotsis, A" sort="Kotsis, A" uniqKey="Kotsis A" first="A." last="Kotsis">A. Kotsis</name>
<affiliation wicri:level="1"><country xml:lang="fr">Grèce</country>
<wicri:regionArea>Department of General Biology, Medical School, Aristotle University of Thessaloniki, Thessaloniki</wicri:regionArea>
<wicri:noRegion>Thessaloniki</wicri:noRegion>
</affiliation>
</author>
</analytic>
<monogr></monogr>
<series><title level="j">European Journal of Neurology</title>
<idno type="ISSN">1351-5101</idno>
<idno type="eISSN">1468-1331</idno>
<imprint><publisher>Blackwell Publishing Ltd</publisher>
<pubPlace>Oxford, UK</pubPlace>
<date type="published" when="2007-10">2007-10</date>
<biblScope unit="volume">14</biblScope>
<biblScope unit="issue">10</biblScope>
<biblScope unit="page" from="1088">1088</biblScope>
<biblScope unit="page" to="1090">1090</biblScope>
</imprint>
<idno type="ISSN">1351-5101</idno>
</series>
<idno type="istex">0E35C463024562ADDCC87D7F105411C10D63BE6A</idno>
<idno type="DOI">10.1111/j.1468-1331.2007.01867.x</idno>
<idno type="ArticleID">ENE1867</idno>
</biblStruct>
</sourceDesc>
<seriesStmt><idno type="ISSN">1351-5101</idno>
</seriesStmt>
</fileDesc>
<profileDesc><textClass><keywords scheme="KwdEn" xml:lang="en"><term>G2019S mutation</term>
<term>LRRK2 gene</term>
<term>sporadic Parkinson's disease</term>
</keywords>
</textClass>
<langUsage><language ident="en">en</language>
</langUsage>
</profileDesc>
</teiHeader>
<front><div type="abstract" xml:lang="en">Parkinson's disease (PD) is the second most common neurodegenerative disorder affecting approximately 2% of the population >60 years of age. Although, the etiology of PD is still unknown, the genetic background of the disease has been documented. Recently, a mutation in the LRRK2 gene, G2019S, was associated with 3–41% and 1–2% of familial and sporadic PD, respectively suggesting a pivotal role of LRRK2 in PD. In this report, we examine the association of the G2019S mutation with sporadic late‐onset PD, in an independent cohort of Greek patients and controls.</div>
</front>
</TEI>
<affiliations><list><country><li>Grèce</li>
</country>
</list>
<tree><country name="Grèce"><noRegion><name sortKey="Kalinderi, K" sort="Kalinderi, K" uniqKey="Kalinderi K" first="K." last="Kalinderi">K. Kalinderi</name>
</noRegion>
<name sortKey="Bostantjopoulou, S" sort="Bostantjopoulou, S" uniqKey="Bostantjopoulou S" first="S." last="Bostantjopoulou">S. Bostantjopoulou</name>
<name sortKey="Fidani, L" sort="Fidani, L" uniqKey="Fidani L" first="L." last="Fidani">L. Fidani</name>
<name sortKey="Katsarou, Z" sort="Katsarou, Z" uniqKey="Katsarou Z" first="Z." last="Katsarou">Z. Katsarou</name>
<name sortKey="Kotsis, A" sort="Kotsis, A" uniqKey="Kotsis A" first="A." last="Kotsis">A. Kotsis</name>
</country>
</tree>
</affiliations>
</record>
Pour manipuler ce document sous Unix (Dilib)
EXPLOR_STEP=$WICRI_ROOT/Wicri/Sante/explor/ParkinsonV1/Data/Main/Exploration
HfdSelect -h $EXPLOR_STEP/biblio.hfd -nk 000F41 | SxmlIndent | more
Ou
HfdSelect -h $EXPLOR_AREA/Data/Main/Exploration/biblio.hfd -nk 000F41 | SxmlIndent | more
Pour mettre un lien sur cette page dans le réseau Wicri
{{Explor lien |wiki= Wicri/Sante |area= ParkinsonV1 |flux= Main |étape= Exploration |type= RBID |clé= ISTEX:0E35C463024562ADDCC87D7F105411C10D63BE6A |texte= The G2019S LRRK2 mutation is uncommon amongst Greek patients with sporadic Parkinson's disease }}
This area was generated with Dilib version V0.6.23. |