Movement Disorders (revue)

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ELAVL4, PARK10, and the Celts

Identifieur interne : 002E75 ( Main/Exploration ); précédent : 002E74; suivant : 002E76

ELAVL4, PARK10, and the Celts

Auteurs : Kristoffer Haugarvoll [États-Unis, Norvège] ; Mathias Toft [États-Unis, Norvège] ; Owen A. Ross [États-Unis] ; Jeremy T. Stone [États-Unis] ; Michael G. Heckman [États-Unis] ; Linda R. White [Norvège] ; Timothy Lynch [Irlande (pays)] ; John Mark Gibson [Irlande (pays)] ; Zbigniew K. Wszolek [États-Unis] ; Ryan J. Uitti [États-Unis] ; Jan O. Aasly [Norvège] ; Matthew J. Farrer [États-Unis]

Source :

RBID : ISTEX:854CA06A79DBF113B64DFF23D15A88F6ADA1C79D

Descripteurs français

English descriptors

Abstract

Genetic variability in ELAVL4 located in the PARK10 locus was recently associated with age‐at‐onset (AAO) in a series of Parkinson's disease (PD) patients originating from the United States. We examined five markers spanning ELAVL4 in Norwegian, United States, and Irish PD case–control samples. No association was found between the examined markers and AAO or PD in Norwegian or US samples. However, ELAVL4 markers (rs967582 and rs3902720) were significantly associated with susceptibility to PD in our Irish series. Our data suggest that the association between ELAVL4 and PD previously observed might be explained by a Celtic‐founder effect. © 2007 Movement Disorder Society

Url:
DOI: 10.1002/mds.21336


Affiliations:


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Le document en format XML

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<term>Adult</term>
<term>Age Factors</term>
<term>Aged</term>
<term>Aged, 80 and over</term>
<term>Alleles</term>
<term>ELAVL4</term>
<term>Female</term>
<term>Genetic Linkage (genetics)</term>
<term>Genetic Markers</term>
<term>Genetic Predisposition to Disease</term>
<term>Hu Paraneoplastic Encephalomyelitis Antigens (genetics)</term>
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<div type="abstract" xml:lang="en">Genetic variability in ELAVL4 located in the PARK10 locus was recently associated with age‐at‐onset (AAO) in a series of Parkinson's disease (PD) patients originating from the United States. We examined five markers spanning ELAVL4 in Norwegian, United States, and Irish PD case–control samples. No association was found between the examined markers and AAO or PD in Norwegian or US samples. However, ELAVL4 markers (rs967582 and rs3902720) were significantly associated with susceptibility to PD in our Irish series. Our data suggest that the association between ELAVL4 and PD previously observed might be explained by a Celtic‐founder effect. © 2007 Movement Disorder Society</div>
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