Congenital myopathy with selective muscle atrophy, necklace-like fibres/central cores and craniosynostosis associated with recessive mutations in SCN4A

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Bibliographic Details
Published in:Neuromuscular disorders : NMD 2016-10, Vol.26, p.S193-S193
Main Authors: Gonorazky, H, Marshall, C, Hazrati, L, Männikkö, R, Ray, P, Yoon, G
Format: Article
Language:English
Subjects:
Neurology
Online Access:Get full text
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ISSN:0960-8966
DOI:10.1016/j.nmd.2016.06.388