Mutations in the Fukutin-Related Protein Gene (FKRP) Cause a Form of Congenital Muscular Dystrophy with Secondary Laminin α2 Deficiency and Abnormal Glycosylation of α-Dystroglycan

✍ Scribed by Martin Brockington; Derek J. Blake; Paola Prandini; Susan C. Brown; Silvia Torelli; Matthew A. Benson; Chris P. Ponting; Brigitte Estournet; Norma B. Romero; Eugenio Mercuri; Thomas Voit; Caroline A. Sewry; Pascale Guicheney; Francesco Muntoni

• Book ID: 117853742
• Publisher: American Society of Human Genetics
• Year: 2001
• Tongue: English
• Weight: 244 KB
• Volume: 69
• Category: Article
• ISSN: 0002-9297
• DOI: 10.1086/324412