The m.5650G>A mitochondrial tRNAAla mutation is pathogenic and causes a phenotype of pure myopathy. (2008)

First Author: McFarland R

Abstract

No abstract provided

Bibliographic Information

Digital Object Identifier: http://dx.doi.org/10.1016/j.nmd.2007.07.007

PubMed Identifier: 17825557

Publication URI: http://europepmc.org/abstract/MED/17825557

Type: Journal Article/Review

Volume: 18

Parent Publication: Neuromuscular disorders : NMD

Issue: 1

ISSN: 0960-8966