Nemaline myopathy 7

MONDO:0012538

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

4 clinical trials for this condition and its sub-types, 0 tagged with Nemaline myopathy 7 itself.

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