Do mutations in the murine ataxia gene TRPC3 cause cerebellar ataxia in humans?
Identifieur interne : 004184 ( Ncbi/Curation ); précédent : 004183; suivant : 004185Do mutations in the murine ataxia gene TRPC3 cause cerebellar ataxia in humans?
Auteurs : Brent L. Fogel [États-Unis] ; Sonya M. Hanson ; Esther B E. BeckerSource :
- Movement disorders : official journal of the Movement Disorder Society [ 1531-8257 ] ; 2015.
English descriptors
- KwdEn :
- MESH :
- chemical , genetics : TRPC Cation Channels.
- diagnosis : Ataxia.
- genetics : Ataxia, Mutation.
- pathology : Brain.
- Adult, Genetic Heterogeneity, Genetic Predisposition to Disease, Humans, Male.
DOI: 10.1002/mds.26096
PubMed: 25477146
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pubmed:25477146Le document en format XML
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<author><name sortKey="Fogel, Brent L" sort="Fogel, Brent L" uniqKey="Fogel B" first="Brent L" last="Fogel">Brent L. Fogel</name>
<affiliation wicri:level="2"><nlm:affiliation>Program in Neurogenetics, Department of Neurology David Geffen School of Medicine, University of California Los Angeles, Los Angeles, California, USA.</nlm:affiliation>
<country xml:lang="fr">États-Unis</country>
<wicri:regionArea>Program in Neurogenetics, Department of Neurology David Geffen School of Medicine, University of California Los Angeles, Los Angeles, California</wicri:regionArea>
<placeName><region type="state">Californie</region>
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<author><name sortKey="Hanson, Sonya M" sort="Hanson, Sonya M" uniqKey="Hanson S" first="Sonya M" last="Hanson">Sonya M. Hanson</name>
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<author><name sortKey="Becker, Esther B E" sort="Becker, Esther B E" uniqKey="Becker E" first="Esther B E" last="Becker">Esther B E. Becker</name>
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<sourceDesc><biblStruct><analytic><title xml:lang="en">Do mutations in the murine ataxia gene TRPC3 cause cerebellar ataxia in humans?</title>
<author><name sortKey="Fogel, Brent L" sort="Fogel, Brent L" uniqKey="Fogel B" first="Brent L" last="Fogel">Brent L. Fogel</name>
<affiliation wicri:level="2"><nlm:affiliation>Program in Neurogenetics, Department of Neurology David Geffen School of Medicine, University of California Los Angeles, Los Angeles, California, USA.</nlm:affiliation>
<country xml:lang="fr">États-Unis</country>
<wicri:regionArea>Program in Neurogenetics, Department of Neurology David Geffen School of Medicine, University of California Los Angeles, Los Angeles, California</wicri:regionArea>
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<author><name sortKey="Becker, Esther B E" sort="Becker, Esther B E" uniqKey="Becker E" first="Esther B E" last="Becker">Esther B E. Becker</name>
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<series><title level="j">Movement disorders : official journal of the Movement Disorder Society</title>
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<imprint><date when="2015" type="published">2015</date>
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<term>Ataxia (diagnosis)</term>
<term>Ataxia (genetics)</term>
<term>Brain (pathology)</term>
<term>Genetic Heterogeneity</term>
<term>Genetic Predisposition to Disease</term>
<term>Humans</term>
<term>Male</term>
<term>Mutation (genetics)</term>
<term>TRPC Cation Channels (genetics)</term>
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<keywords scheme="MESH" type="chemical" qualifier="genetics" xml:lang="en"><term>TRPC Cation Channels</term>
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<keywords scheme="MESH" qualifier="diagnosis" xml:lang="en"><term>Ataxia</term>
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<keywords scheme="MESH" qualifier="genetics" xml:lang="en"><term>Ataxia</term>
<term>Mutation</term>
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<keywords scheme="MESH" xml:lang="en"><term>Adult</term>
<term>Genetic Heterogeneity</term>
<term>Genetic Predisposition to Disease</term>
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