POMT1 and POMT2 gene mutations result in 2 cases of alpha- dystroglycanopathy
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Alpha-dystroglycanopathy (α-DGP) is a group of congenital muscular dystrophy and limb band muscular dystrophy caused by abnormal glycosylation of α-dystroglycan (α-DG). At present, there are few studies on the clinical manifestations, genetic characteristic... ...