Mutations in hippocalcin and autosomal recessive dystonia: a role for perturbed calcium signaling?
Identifieur interne : 000158 ( Main/Exploration ); précédent : 000157; suivant : 000159Mutations in hippocalcin and autosomal recessive dystonia: a role for perturbed calcium signaling?
Auteurs : Kishore Raj Kumar [Australie]Source :
- Movement disorders : official journal of the Movement Disorder Society [ 1531-8257 ] ; 2015.
English descriptors
- KwdEn :
- MESH :
- chemical , genetics : Hippocalcin.
- genetics : Dystonia, Genes, Recessive, Mutation.
- Humans.
DOI: 10.1002/mds.26261
PubMed: 26009984
Affiliations:
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Le document en format XML
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<author><name sortKey="Kumar, Kishore Raj" sort="Kumar, Kishore Raj" uniqKey="Kumar K" first="Kishore Raj" last="Kumar">Kishore Raj Kumar</name>
<affiliation wicri:level="1"><nlm:affiliation>Department of Neurology and Neurogenetics, Kolling Institute of Medical Research, Royal North Shore Hospital and The University of Sydney, St Leonards, NSW, Australia.</nlm:affiliation>
<country xml:lang="fr">Australie</country>
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<author><name sortKey="Kumar, Kishore Raj" sort="Kumar, Kishore Raj" uniqKey="Kumar K" first="Kishore Raj" last="Kumar">Kishore Raj Kumar</name>
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<country xml:lang="fr">Australie</country>
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<series><title level="j">Movement disorders : official journal of the Movement Disorder Society</title>
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<profileDesc><textClass><keywords scheme="KwdEn" xml:lang="en"><term>Dystonia (genetics)</term>
<term>Genes, Recessive (genetics)</term>
<term>Hippocalcin (genetics)</term>
<term>Humans</term>
<term>Mutation (genetics)</term>
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<keywords scheme="MESH" type="chemical" qualifier="genetics" xml:lang="en"><term>Hippocalcin</term>
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<keywords scheme="MESH" qualifier="genetics" xml:lang="en"><term>Dystonia</term>
<term>Genes, Recessive</term>
<term>Mutation</term>
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