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Bi-allelic mutations in MYL1 cause a severe congenital myopathy. (2018)

First Author: Ravenscroft G

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

Abstract

No abstract provided

Bibliographic Information

Digital Object Identifier: http://dx.doi.org/10.1093/hmg/ddy320

PubMed Identifier: 30215711

Publication URI: http://europepmc.org/abstract/MED/30215711

Type: Journal Article/Review

Volume: 27

Parent Publication: Human molecular genetics

Issue: 24

ISSN: 0964-6906