Mystery surrounding DYT2 dystonia now solved: HPCA mutations identified in DYT2-like family.
Identifieur interne : 000156 ( Main/Exploration ); précédent : 000155; suivant : 000157Mystery surrounding DYT2 dystonia now solved: HPCA mutations identified in DYT2-like family.
Auteurs : Franziska Hopfner [Allemagne] ; Susanne A. Schneider [Allemagne]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.26288
PubMed: 26095160
Affiliations:
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Le document en format XML
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