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Mutations in B3GALNT2 cause congenital muscular dystrophy and hypoglycosylation of a-dystroglycan. (2013)

First Author: Stevens E

Attributed to: MICA: MRC Centre for Neuromuscular Diseases funded by MRC

Abstract

No abstract provided

Bibliographic Information

Digital Object Identifier: http://dx.doi.org/10.1016/j.ajhg.2013.01.016

PubMed Identifier: 23453667

Publication URI: http://europepmc.org/abstract/MED/23453667

Type: Journal Article/Review

Volume: 92

Parent Publication: American journal of human genetics

Issue: 3

ISSN: 0002-9297