Clinical, histological and genetic characterization of reducing body myopathy caused by mutations in FHL1. (2009)

First Author: Schessl J

Abstract

No abstract provided

Bibliographic Information

Digital Object Identifier: http://dx.doi.org/10.1093/brain/awn325

PubMed Identifier: 19181672

Publication URI: http://europepmc.org/abstract/MED/19181672

Type: Journal Article/Review

Volume: 132

Parent Publication: Brain : a journal of neurology

Issue: Pt 2

ISSN: 0006-8950