Associated Papers
Novel POMGnT1 mutations define broader phenotypic spectrum of muscle-eye-brain disease.
Hehr U et al.
Neurogenetics, 2007
Congenital muscular dystrophy with glycosylation defects of alpha-dystroglycan in Japan.
Matsumoto H et al.
Neuromuscular Disorders : Nmd, 2005
Glycosylation in congenital muscular dystrophies.
Endo T et al.
Biological & Pharmaceutical Bulletin, 2003
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