Nemaline myopathy 9

MONDO:0014326

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

4 clinical trials for this condition and its sub-types, 0 tagged with Nemaline myopathy 9 itself.

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