G309D and W437OPA PINK1 mutations in Caucasian Parkinson's disease patients.
Identifieur interne : 000091 ( Ncbi/Checkpoint ); précédent : 000090; suivant : 000092G309D and W437OPA PINK1 mutations in Caucasian Parkinson's disease patients.
Auteurs : H. Deng [États-Unis] ; W Le ; X. Zhang ; T Pan ; Joseph Jankovic [États-Unis]Source :
- Acta neurologica Scandinavica [ 0001-6314 ] ; 2005.
Descripteurs français
- Wicri :
- geographic : États-Unis.
English descriptors
- KwdEn :
- Adult, Amino Acid Substitution, DNA Mutational Analysis, European Continental Ancestry Group (genetics), Female, Genetic Testing, Genome, Human, Humans, Male, Middle Aged, Mutation (genetics), Parkinson Disease (ethnology), Parkinson Disease (genetics), Parkinson Disease (metabolism), Protein Kinases (genetics), United States.
- 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
To determine whether the G309D and W437OPA mutations in PINK1 gene are present in American Caucasian population of patients with Parkinson's disease (PD).
DOI: 10.1111/j.1600-0404.2005.00383.x
PubMed: 15876334
Affiliations:
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- to stream Ncbi, to step Merge: 000091
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pubmed:15876334Le document en format XML
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<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>
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<author><name sortKey="Le, W D" sort="Le, W D" uniqKey="Le W" first="W" last="Le">W Le</name>
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<author><name sortKey="Zhang, X" sort="Zhang, X" uniqKey="Zhang X" first="X" last="Zhang">X. Zhang</name>
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<author><name sortKey="Pan, T H" sort="Pan, T H" uniqKey="Pan T" first="T" last="Pan">T Pan</name>
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<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>
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<orgName type="university" n="3">Baylor College of Medicine</orgName>
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<sourceDesc><biblStruct><analytic><title xml:lang="en">G309D and W437OPA PINK1 mutations in Caucasian Parkinson's disease patients.</title>
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<author><name sortKey="Zhang, X" sort="Zhang, X" uniqKey="Zhang X" first="X" last="Zhang">X. Zhang</name>
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<author><name sortKey="Pan, T H" sort="Pan, T H" uniqKey="Pan T" first="T" last="Pan">T Pan</name>
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<author><name sortKey="Jankovic, J" sort="Jankovic, J" uniqKey="Jankovic J" first="J" last="Jankovic">Joseph Jankovic</name>
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<series><title level="j">Acta neurologica Scandinavica</title>
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<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>
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<keywords scheme="MESH" type="chemical" qualifier="genetics" xml:lang="en"><term>Protein Kinases</term>
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<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>
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<keywords scheme="MESH" qualifier="metabolism" xml:lang="en"><term>Parkinson Disease</term>
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<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>
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<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>
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<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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<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">Joseph Jankovic</name>
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