Late-onset axial myopathy with cores due to a novel heterozygous dominant mutation in the skeletal muscle ryanodine receptor (RYR1) gene. (2009)

First Author: Jungbluth H


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Bibliographic Information

Digital Object Identifier:

PubMed Identifier: 19303294

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Type: Journal Article/Review

Volume: 19

Parent Publication: Neuromuscular disorders : NMD

Issue: 5

ISSN: 0960-8966