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


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Bibliographic Information

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PubMed Identifier: 23453667

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Type: Journal Article/Review

Volume: 92

Parent Publication: American journal of human genetics

Issue: 3

ISSN: 0002-9297