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Echinobase
Summary Literature (0)
MIM:609308 - MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (LIMB-GIRDLE), TYPE C, 1; MDDGC1

Echinobase Genes: pomt1

Human Disease Resource: MIM


Disease Ontology (DO):
DOID:0110297 - autosomal recessive limb-girdle muscular dystrophy type 2K