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Novel mutations widen the phenotypic spectrum of slow skeletal/ß-cardiac myosin (MYH7) distal myopathy. (2014)

First Author: Lamont PJ

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.22553

PubMed Identifier: 24664454

Publication URI: http://europepmc.org/abstract/MED/24664454

Type: Journal Article/Review

Volume: 35

Parent Publication: Human mutation

Issue: 7

ISSN: 1059-7794