ISPD gene mutations are a common cause of congenital and limb-girdle muscular dystrophies. (2013)

First Author: Cirak S
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/brain/aws312

PubMed Identifier: 23288328

Publication URI: http://europepmc.org/abstract/MED/23288328

Type: Journal Article/Review

Volume: 136

Parent Publication: Brain : a journal of neurology

Issue: Pt 1

ISSN: 0006-8950