Ryanodine receptor type 3 (RYR3) as a novel gene associated with nemaline myopathy and fibre type disproportion

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Bibliographic Details
Published in:Neuromuscular disorders : NMD 2016-10, Vol.26, p.S137-S137
Main Authors: Nilipour, Y, Nafissi, S, Varasteh, V, Hossein-Nejad, H, Tonekaboni, S, Ravenscroft, G, Olivé, M, Laing, N, Tajsharghi, H
Format: Article
Language:English
Subjects:
Neurology
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ISSN:0960-8966
DOI:10.1016/j.nmd.2016.06.188