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RyR1 deficiency in congenital myopathies disrupts excitation-contraction coupling. (2013)

First Author: Zhou H

Attributed to: MICA: MRC Centre for Neuromuscular Diseases funded by MRC

Abstract

No abstract provided

Bibliographic Information

Digital Object Identifier: http://dx.doi.org/10.1002/humu.22326

PubMed Identifier: 23553787

Publication URI: http://europepmc.org/abstract/MED/23553787

Type: Journal Article/Review

Volume: 34

Parent Publication: Human mutation

Issue: 7

ISSN: 1059-7794