Orphanet Journal of Rare Diseases BioMed Central

First Page		Document Content
Congenital muscular dystrophy Fukutin Dystroglycan POMT1 Laminin Neuronal migration disorder POMT2 Dystrophin Fukuyama congenital muscular dystrophy Health Muscular dystrophy Walker–Warburg syndrome		Orphanet Journal of Rare Diseases BioMed Central Add to Reading List Source URL: www.ojrd.com Download Document from Source Website File Size: 259,78 KB Share Document on Facebook

	NEWS & VIEWS RESEARCH descendants of this particular event probably suffered no harm, because disrupting one copy of fukutin has no adverse effects. The consequences for modern Japan, however, are quite different. Around DocID: GwW2 - View Document
	Neuromuscular Disorders[removed]–649 www.elsevier.com/locate/nmd Review The congenital muscular dystrophies in 2004: DocID: zOUT - View Document
	Overview: Dystroglycan is a major component of the dystrophin-glycoprotein complex (DGC) acting as a transmembrane bridge across the sarcolemmal membrane. Dystroglycan binds to laminin (mediated by O-linked glycosylation DocID: zBaQ - View Document
	CMLS, Cell. Mol. Life Sci[removed]– [removed]682X[removed]DOI[removed]s00018[removed] © Birkhäuser Verlag, Basel, 2005 CMLS DocID: zzsz - View Document
	Global FKRP Patient Registry Newsletter Issue 1 April 2012 DocID: zwII - View Document