COQ2 gene variants associate with cerebellar subtype of multiple system atrophy in Chinese.
Identifieur interne : 000305 ( Main/Exploration ); précédent : 000304; suivant : 000306COQ2 gene variants associate with cerebellar subtype of multiple system atrophy in Chinese.
Auteurs : Chin-Hsien Lin [Taïwan] ; Eng-King Tan ; Chih-Chao Yang ; Zhao Yi ; Ruey-Meei WuSource :
- Movement disorders : official journal of the Movement Disorder Society [ 1531-8257 ] ; 2015.
DOI: 10.1002/mds.26138
PubMed: 25594503
Affiliations:
Links toward previous steps (curation, corpus...)
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- to stream Ncbi, to step Curation: 004218
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Le document en format XML
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<author><name sortKey="Lin, Chin Hsien" sort="Lin, Chin Hsien" uniqKey="Lin C" first="Chin-Hsien" last="Lin">Chin-Hsien Lin</name>
<affiliation wicri:level="1"><nlm:affiliation>Department of Neurology, National Taiwan University Hospital, College of Medicine, National Taiwan University, Taipei, Taiwan.</nlm:affiliation>
<country xml:lang="fr">Taïwan</country>
<wicri:regionArea>Department of Neurology, National Taiwan University Hospital, College of Medicine, National Taiwan University, Taipei</wicri:regionArea>
<wicri:noRegion>Taipei</wicri:noRegion>
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<author><name sortKey="Tan, Eng King" sort="Tan, Eng King" uniqKey="Tan E" first="Eng-King" last="Tan">Eng-King Tan</name>
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<author><name sortKey="Yang, Chih Chao" sort="Yang, Chih Chao" uniqKey="Yang C" first="Chih-Chao" last="Yang">Chih-Chao Yang</name>
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<author><name sortKey="Yi, Zhao" sort="Yi, Zhao" uniqKey="Yi Z" first="Zhao" last="Yi">Zhao Yi</name>
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<series><title level="j">Movement disorders : official journal of the Movement Disorder Society</title>
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