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

Mutations in B3GALNT2 Cause Congenital Muscular Dystrophy and Hypoglycosylation of α-Dystroglycan http://www.deepdyve.com/assets/images/DeepDyve-Logo-lg.png The American Journal of Human Genetics Unpaywall
 
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References (53)

Publisher
Unpaywall
ISSN
0002-9297
DOI
10.1016/j.ajhg.2013.01.016
Publisher site
See Article on Publisher Site

Abstract

Journal

The American Journal of Human GeneticsUnpaywall

Published: Feb 28, 2013

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