Mutations in B3GALNT2 Cause Congenital Muscular Dystrophy and Hypoglycosylation of alpha-Dystroglycan

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Published Version
Embargoed until: 2100-01-01

Volume

92

Pagination

354 - 365

DOI

10.1016/j.ajhg.2013.01.016

Journal

AMERICAN JOURNAL OF HUMAN GENETICS

Issue

3

ISSN

0002-9297

Metadata

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Authors

Stevens, E; Carss, KJ; Cirak, S; Foley, R; Torelli, S; Willer, T; Tambunan, DE; Yau, S; Brodd, L; Sewry, CA

URI

http://qmro.qmul.ac.uk/xmlui/handle/123456789/15141

Collections

Centre for Genomics and Child Health [778]

Licence information

http://dx.doi.org/10.1016/j.ajhg.2013.01.016

Copyright statements

Copyright © 2013 The American Society of Human Genetics