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Novel myosin-based therapies for congenital cardiac and skeletal myopathies. (2016)

First Author: Ochala J

Attributed to: Determining how mutations in actin lead to skeletal muscle weakness funded by MRC

Abstract

No abstract provided

Bibliographic Information

Digital Object Identifier: http://dx.doi.org/10.1136/jmedgenet-2016-103881

PubMed Identifier: 27412953

Publication URI: http://europepmc.org/abstract/MED/27412953

Type: Journal Article/Review

Volume: 53

Parent Publication: Journal of medical genetics

Issue: 10

ISSN: 0022-2593