Nemaline myopathy 7

Any nemaline myopathy in which the cause of the disease is a mutation in the CFL2 gene.

Also known as: CFL2 nemaline myopathy, NEM7, nemaline myopathy 7, nemaline myopathy caused by mutation in CFL2, nemaline myopathy type 7

37 clinical trials for this condition and its sub-types.