The dystroglycanopathies: The new disorders of o-linked glycosylation

Seminars in Pediatric Neurology

Volumn 12, Issue 3, 2005, Pages 152-158

  Martin, Paul T ^a  

^a THE OHIO STATE UNIVERSITY COLLEGE OF MEDICINE   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

CARBOHYDRATE; CELL ADHESION MOLECULE; DYSTROGLYCAN; FUKUTIN; GLYCOSAMINOGLYCAN; GLYCOSYLTRANSFERASE; NITROGEN; OXYGEN; SCLEROPROTEIN;

BRAIN; CLINICAL FEATURE; CONGENITAL DISORDER OF GLYCOSYLATION; DIAGNOSTIC TEST; EYE; FUKUYAMA CONGENITAL MUSCULAR DYSTROPHY; GENE MUTATION; GLYCOSYLATION; HUMAN; LIMB GIRDLE MUSCULAR DYSTROPHY; MUSCLE; MUSCLE EYE BRAIN DISEASE; MUSCULAR DYSTROPHY; NONHUMAN; PHENOTYPE; PROTEIN BINDING; PROTEIN DEFECT; PROTEIN EXPRESSION; REVIEW; WALKER WARBURG SYNDROME;

DYSTROGLYCANS; GENE EXPRESSION; GLYCOSYLATION; HUMANS; MUSCULAR DYSTROPHIES; POINT MUTATION;

EID: 33644745063     PISSN: 10719091     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.spen.2005.10.003     Document Type: Review

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