Nemaline Myopathy 9 (NEM9)

Nemaline Myopathy 9, also known as nem9, is related to nemaline myopathy and childhood-onset nemaline myopathy, and has symptoms including muscle weakness An important gene associated with Nemaline Myopathy 9 is KLHL41 (Kelch Like Family Member 41). Affiliated tissues include skeletal muscle, and related phenotypes are respiratory insufficiency and fetal akinesia sequence