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Contraindications Wilson's disease: A genetic disorder that causes copper to accumulate in organs
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Dystroglycanopathies are primarily linked mutations in glycosyltransferases that target α-dystroglycan, including fukutin-related protein ( FKRP /LGMD2I) [139], fukutin ( FKTN /LGMD2M), -like-acetylglucosaminyl transferase ( LARGE ), protein-O-mannosyltransferase 1 ( POMT1 /LGMD2K), protein-O-mannosyl transferase 2 ( POMT2 /LGMD2N), protein-O-mannose-1,2-N-acetylglucosaminyltransferase 1 ( POMGNT1 /LGMD2O), dolichyl-phosphate mannosyltransferase polypeptide 3 ( DPM3 ), and isoprenoid synthase domain containing ( ISPD /LGMD2U) [151,152,153,154,155,156]
