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Myoclonus dystonia and muscular dystrophy: ɛ‐sarcoglycan is part of the dystrophin‐associated protein complex in brain

BACKGROUND: Myoclonus‐dystonia is a neurogenic movement disorder caused by mutations in the gene encoding ɛ‐sarcoglycan. By contrast, mutations in the α‐, β‐, γ‐, and δ‐sarcoglycan genes cause limb girdle muscular dystrophies. The sarcoglycans are part of the dystrophin‐associated protein complex in...

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Bibliografiske detaljer
Udgivet i:Mov Disord
Main Authors: Waite, Adrian J., Carlisle, Francesca A., Chan, Yiumo Michael, Blake, Derek J.
Format: Artigo
Sprog:Inglês
Udgivet: John Wiley and Sons Inc. 2016
Fag:
Online adgang:https://ncbi.nlm.nih.gov/pmc/articles/PMC5129563/
https://ncbi.nlm.nih.gov/pubmed/27535350
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1002/mds.26738
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