Associated Papers
Novel POMGnT1 mutations define broader phenotypic spectrum of muscle-eye-brain disease.
Hehr U et al.
Neurogenetics, 2007
Glycosylation in congenital muscular dystrophies.
Endo T et al.
Biological & Pharmaceutical Bulletin, 2003
Worldwide distribution and broader clinical spectrum of muscle-eye-brain disease.
Taniguchi K et al.
Human Molecular Genetics, 2003
Muscular dystrophy and neuronal migration disorder caused by mutations in a glycosyltransferase, POMGnT1.
Yoshida A et al.
Developmental Cell, 2001
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