Browse
Explore conditions, clinical trials, and the organisations running them.
Up to: Childhood-onset nemaline myopathy · Severe congenital nemaline myopathy · Intermediate nemaline myopathy · Typical nemaline myopathy
Nemaline myopathy 9
Any nemaline myopathy in which the cause of the disease is a mutation in the KLHL41 gene.
This condition has no sub-types.