Genetic and clinical identification of Parkinson's disease patients with LRRK2 G2019S mutation.
Identifieur interne : 000092 ( Ncbi/Merge ); précédent : 000091; suivant : 000093Genetic and clinical identification of Parkinson's disease patients with LRRK2 G2019S mutation.
Auteurs : Hao Deng ; Weidong Le ; Yi Guo ; Christine. Hunter ; Wenjie Xie ; Joseph Jankovic [États-Unis]Source :
- Annals of neurology [ 0364-5134 ] ; 2005.
English descriptors
- KwdEn :
- MESH :
- chemical , genetics : Protein-Serine-Threonine Kinases.
- geographic : North America.
- genetics : Parkinson Disease.
- Aged, Female, Humans, Male, Middle Aged, Point Mutation.
DOI: 10.1002/ana.20510
PubMed: 15929036
Links toward previous steps (curation, corpus...)
- to stream PubMed, to step Corpus: 000197
- to stream PubMed, to step Curation: 000197
- to stream PubMed, to step Checkpoint: 000195
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pubmed:15929036Le document en format XML
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<author><name sortKey="Deng, Hao" sort="Deng, Hao" uniqKey="Deng H" first="Hao" last="Deng">Hao Deng</name>
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<author><name sortKey="Le, Weidong" sort="Le, Weidong" uniqKey="Le W" first="Weidong" last="Le">Weidong Le</name>
</author>
<author><name sortKey="Guo, Yi" sort="Guo, Yi" uniqKey="Guo Y" first="Yi" last="Guo">Yi Guo</name>
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<author><name sortKey="Hunter, Christine B" sort="Hunter, Christine B" uniqKey="Hunter C" first="Christine" last="Hunter">Christine. Hunter</name>
</author>
<author><name sortKey="Xie, Wenjie" sort="Xie, Wenjie" uniqKey="Xie W" first="Wenjie" last="Xie">Wenjie Xie</name>
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<author><name sortKey="Jankovic, Joseph" sort="Jankovic, Joseph" uniqKey="Jankovic J" first="Joseph" last="Jankovic">Joseph Jankovic</name>
<affiliation><country>États-Unis</country>
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<region type="state">Texas</region>
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<author><name sortKey="Le, Weidong" sort="Le, Weidong" uniqKey="Le W" first="Weidong" last="Le">Weidong Le</name>
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<author><name sortKey="Guo, Yi" sort="Guo, Yi" uniqKey="Guo Y" first="Yi" last="Guo">Yi Guo</name>
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<author><name sortKey="Hunter, Christine B" sort="Hunter, Christine B" uniqKey="Hunter C" first="Christine" last="Hunter">Christine. Hunter</name>
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<author><name sortKey="Xie, Wenjie" sort="Xie, Wenjie" uniqKey="Xie W" first="Wenjie" last="Xie">Wenjie Xie</name>
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<author><name sortKey="Jankovic, Joseph" sort="Jankovic, Joseph" uniqKey="Jankovic J" first="Joseph" last="Jankovic">Joseph Jankovic</name>
<affiliation><country>États-Unis</country>
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<series><title level="j">Annals of neurology</title>
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<term>Middle Aged</term>
<term>North America</term>
<term>Parkinson Disease (genetics)</term>
<term>Point Mutation</term>
<term>Protein-Serine-Threonine Kinases (genetics)</term>
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<keywords scheme="MESH" type="chemical" qualifier="genetics" xml:lang="en"><term>Protein-Serine-Threonine Kinases</term>
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<keywords scheme="MESH" type="geographic" xml:lang="en"><term>North America</term>
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<keywords scheme="MESH" qualifier="genetics" xml:lang="en"><term>Parkinson Disease</term>
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<keywords scheme="MESH" xml:lang="en"><term>Aged</term>
<term>Female</term>
<term>Humans</term>
<term>Male</term>
<term>Middle Aged</term>
<term>Point Mutation</term>
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<Month>06</Month>
<Day>06</Day>
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<DateCompleted><Year>2005</Year>
<Month>07</Month>
<Day>26</Day>
</DateCompleted>
<DateRevised><Year>2012</Year>
<Month>06</Month>
<Day>25</Day>
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<Article PubModel="Print"><Journal><ISSN IssnType="Print">0364-5134</ISSN>
<JournalIssue CitedMedium="Print"><Volume>57</Volume>
<Issue>6</Issue>
<PubDate><Year>2005</Year>
<Month>Jun</Month>
</PubDate>
</JournalIssue>
<Title>Annals of neurology</Title>
<ISOAbbreviation>Ann. Neurol.</ISOAbbreviation>
</Journal>
<ArticleTitle>Genetic and clinical identification of Parkinson's disease patients with LRRK2 G2019S mutation.</ArticleTitle>
<Pagination><MedlinePgn>933-4</MedlinePgn>
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<AuthorList CompleteYN="Y"><Author ValidYN="Y"><LastName>Deng</LastName>
<ForeName>Hao</ForeName>
<Initials>H</Initials>
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<Language>eng</Language>
<GrantList CompleteYN="Y"><Grant><GrantID>NS 043567</GrantID>
<Acronym>NS</Acronym>
<Agency>NINDS NIH HHS</Agency>
<Country>United States</Country>
</Grant>
<Grant><GrantID>NS 40370</GrantID>
<Acronym>NS</Acronym>
<Agency>NINDS NIH HHS</Agency>
<Country>United States</Country>
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<MedlineJournalInfo><Country>United States</Country>
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<MeshHeading><DescriptorName MajorTopicYN="Y" UI="D017354">Point Mutation</DescriptorName>
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<affiliations><list><country><li>États-Unis</li>
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<settlement><li>Houston</li>
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<name sortKey="Hunter, Christine B" sort="Hunter, Christine B" uniqKey="Hunter C" first="Christine" last="Hunter">Christine. Hunter</name>
<name sortKey="Le, Weidong" sort="Le, Weidong" uniqKey="Le W" first="Weidong" last="Le">Weidong Le</name>
<name sortKey="Xie, Wenjie" sort="Xie, Wenjie" uniqKey="Xie W" first="Wenjie" last="Xie">Wenjie Xie</name>
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