Nemaline myopathy 10

Any nemaline myopathy in which the cause of the disease is a mutation in the LMOD3 gene.

Also known as: LMOD3 nemaline myopathy, NEM10, nemaline myopathy 10, nemaline myopathy caused by mutation in LMOD3, nemaline myopathy type 10

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