A novel mutation in the myotilin gene (MYOT) causes a severe form of limb girdle muscular dystrophy 1A (LGMD1A). (2011)

First Author: Reilich P

Abstract

No abstract provided

Bibliographic Information

Digital Object Identifier: http://dx.doi.org/10.1007/s00415-011-5953-9

PubMed Identifier: 21336781

Publication URI: http://europepmc.org/abstract/MED/21336781

Type: Journal Article/Review

Volume: 258

Parent Publication: Journal of neurology

Issue: 8

ISSN: 0340-5354