Muscular dystrophy with large mitochondria associated with mutations in the CHKB gene in three British patients: extending the clinical and pathological phenotype. (2013)

First Author: Quinlivan R
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.nmd.2013.04.002

PubMed Identifier: 23692895

Publication URI: http://europepmc.org/abstract/MED/23692895

Type: Journal Article/Review

Volume: 23

Parent Publication: Neuromuscular disorders : NMD

Issue: 7

ISSN: 0960-8966