Recessive mutations in RYR1 are a common cause of congenital fiber type disproportion. (2010)

First Author: Clarke NF

Abstract

No abstract provided

Bibliographic Information

Digital Object Identifier: http://dx.doi.org/10.1002/humu.21278

PubMed Identifier: 20583297

Publication URI: http://europepmc.org/abstract/MED/20583297

Type: Journal Article/Review

Volume: 31

Parent Publication: Human mutation

Issue: 7

ISSN: 1059-7794