The COQ2 mutations in Japanese multiple system atrophy: impact on the pathogenesis and phenotypic variation.
Identifieur interne : 000403 ( Main/Exploration ); précédent : 000402; suivant : 000404The COQ2 mutations in Japanese multiple system atrophy: impact on the pathogenesis and phenotypic variation.
Auteurs : Tetsutaro Ozawa [Japon]Source :
- Movement disorders : official journal of the Movement Disorder Society [ 1531-8257 ] ; 2014.
English descriptors
- KwdEn :
- MESH :
- chemical , genetics : Alkyl and Aryl Transferases.
- genetics : Multiple System Atrophy.
- Female, Humans, Male.
DOI: 10.1002/mds.25685
PubMed: 24375810
Affiliations:
Links toward previous steps (curation, corpus...)
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- to stream PubMed, to step Curation: 000627
- to stream PubMed, to step Checkpoint: 000405
- to stream Ncbi, to step Merge: 003E70
- to stream Ncbi, to step Curation: 003E70
- to stream Ncbi, to step Checkpoint: 003E70
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Le document en format XML
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<author><name sortKey="Ozawa, Tetsutaro" sort="Ozawa, Tetsutaro" uniqKey="Ozawa T" first="Tetsutaro" last="Ozawa">Tetsutaro Ozawa</name>
<affiliation wicri:level="1"><nlm:affiliation>Department of Neurology, Brain Research Institute, Niigata University, Niigata, Japan.</nlm:affiliation>
<country xml:lang="fr">Japon</country>
<wicri:regionArea>Department of Neurology, Brain Research Institute, Niigata University, Niigata</wicri:regionArea>
<wicri:noRegion>Niigata</wicri:noRegion>
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<sourceDesc><biblStruct><analytic><title xml:lang="en">The COQ2 mutations in Japanese multiple system atrophy: impact on the pathogenesis and phenotypic variation.</title>
<author><name sortKey="Ozawa, Tetsutaro" sort="Ozawa, Tetsutaro" uniqKey="Ozawa T" first="Tetsutaro" last="Ozawa">Tetsutaro Ozawa</name>
<affiliation wicri:level="1"><nlm:affiliation>Department of Neurology, Brain Research Institute, Niigata University, Niigata, Japan.</nlm:affiliation>
<country xml:lang="fr">Japon</country>
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<wicri:noRegion>Niigata</wicri:noRegion>
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<series><title level="j">Movement disorders : official journal of the Movement Disorder Society</title>
<idno type="eISSN">1531-8257</idno>
<imprint><date when="2014" type="published">2014</date>
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<profileDesc><textClass><keywords scheme="KwdEn" xml:lang="en"><term>Alkyl and Aryl Transferases (genetics)</term>
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<term>Humans</term>
<term>Male</term>
<term>Multiple System Atrophy (genetics)</term>
</keywords>
<keywords scheme="MESH" type="chemical" qualifier="genetics" xml:lang="en"><term>Alkyl and Aryl Transferases</term>
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<keywords scheme="MESH" qualifier="genetics" xml:lang="en"><term>Multiple System Atrophy</term>
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<keywords scheme="MESH" xml:lang="en"><term>Female</term>
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<term>Male</term>
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