Nemaline myopathy 9

Any nemaline myopathy in which the cause of the disease is a mutation in the KLHL41 gene.

Also known as: KLHL41 nemaline myopathy, NEM9, nemaline myopathy 9, nemaline myopathy caused by mutation in KLHL41, nemaline myopathy type 9

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