Mutations in KLHL40 are a frequent cause of severe autosomal-recessive nemaline myopathy. (2013)

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/10.1016/j.ajhg.2013.05.004

PubMed Identifier: 23746549

Publication URI: http://europepmc.org/abstract/MED/23746549

Type: Journal Article/Review

Volume: 93

Parent Publication: American journal of human genetics

Issue: 1

ISSN: 0002-9297