Human genes for Becker muscular dystrophy
Becker muscular dystrophy [DOID:9883]
A muscular dystrophy that involves slowly worsening muscle weakness of the legs and pelvis, and has_material_basis in X-linked recessive inheritance of mutation in the dystrophin gene on chromosome Xp21.
Synonyms: Becker muscular dystrophy, Becker muscular dystrophies, DOID:9883, benign congenital myopathy, Benign pseudohypertrophic muscular dystrophy ...
Linkouts: OMIM