Distinct expression of functionally glycosylated alpha-dystroglycan in muscle and non-muscle tissues of FKRP mutant mice
Author:
Funder
Carolinas HealthCare Foundation
Publisher
Public Library of Science (PLoS)
Subject
Multidisciplinary
Reference39 articles.
1. Congenital muscular dystrophies involving the O-mannose pathway;PT Martin;Curr Mol Med,2007
2. ISPD loss-of-function mutations disrupt dystroglycan O-mannosylation and cause Walker-Warburg syndrome;T Willer;Nat Genet,2012
3. Identification of mutations in TMEM5 and ISPD as a cause of severe cobblestone lissencephaly;S Vuillaumier-Barrot;Am J Hum Genet,2012
4. Missense mutations in beta-1,3-N-acetylglucosaminyltransferase 1 (B3GNT1) cause Walker-Warburg syndrome;K Buysse;Hum Mol Genet,2013
5. Exome sequencing and functional validation in zebrafish identify GTDC2 mutations as a cause of Walker-Warburg syndrome;MC Manzini;Am J Hum Genet,2012
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