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MIM:615181 - MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH BRAIN AND EYE ANOMALIES), TYPE A, 11; MDDGA11
Xenbase Genes: b3galnt2
Human Disease Resource: OMIM
DOID:0050588 - muscular dystrophy-dystroglycanopathy type B1 |
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DOID:0050588 - muscular dystrophy-dystroglycanopathy type B1 |