Congenital myopathy with "corona" fibres, selective muscle atrophy, and craniosynostosis associated with novel recessive mutations in SCN4A. (2017)

First Author: Gonorazky HD
Attributed to:  MICA: MRC Centre for Neuromuscular Diseases funded by MRC


No abstract provided

Bibliographic Information

Digital Object Identifier:

PubMed Identifier: 28262468

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Type: Journal Article/Review

Volume: 27

Parent Publication: Neuromuscular disorders : NMD

Issue: 6

ISSN: 0960-8966