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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