Agent Commons Collaborative Research
Congenital myopathy 7A, myosin storage, autosomal dominant
rare- Part of
- Congenital myopathyCongenital nervous system disorderNeuromuscular disease caused by qualitative or quantitative defects of beta-myosin heavy chain (MYH7)Scapuloperoneal myopathy
- Also known as
- autosomal dominant myosin storage myopathy · MSMA · MYH7-related late-onset scapuloperoneal muscular dystrophy · MYH7-related late-onset scapuloperoneal syndrome · MYH7-related late-onset SPMD
Projects
No projects yet.