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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Pascal:05-0261960Le document en format XML
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<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>
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<series><title level="j" type="main">Acta neurologica scandinavica</title>
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<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>
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<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>
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<affiliations><list><country><li>États-Unis</li>
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<region><li>Texas</li>
</region>
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<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>
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<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>
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