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MIM:609115 - MUSCULAR DYSTROPHY, LIMB-GIRDLE, AUTOSOMAL DOMINANT 3; LGMDD3
Xenbase Genes: hnrnpdl
Human Disease Resource: MIM
MONDO:0012193 - autosomal dominant limb-girdle muscular dystrophy type 1G |
DOID:0110306 - autosomal dominant limb-girdle muscular dystrophy type 3 |