Nebulin (NEB) mutations in a childhood onset distal myopathy with rods and cores uncovered by next generation sequencing. (2013)

First Author: Scoto M
Attributed to:  MICA: MRC Centre for Neuromuscular Diseases funded by MRC

Abstract

No abstract provided

Bibliographic Information

Digital Object Identifier: http://dx.doi.org/10.1038/ejhg.2013.31

PubMed Identifier: 23443021

Publication URI: http://europepmc.org/abstract/MED/23443021

Type: Journal Article/Review

Volume: 21

Parent Publication: European journal of human genetics : EJHG

Issue: 11

ISSN: 1018-4813