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


No abstract provided

Bibliographic Information

Digital Object Identifier:

PubMed Identifier: 23443021

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Type: Journal Article/Review

Volume: 21

Parent Publication: European journal of human genetics : EJHG

Issue: 11

ISSN: 1018-4813