In addition, it was reported that recessive small deletions and missense changes in Klhl41 in zebrafish and KLHL41 in humans are linked to diminished motor function, myofibrillar disorganization, and nemaline body formation, which are indicative of nemaline myopathy, whereas frame-shift mutations in the gene could lead to neonatal lethality [95]. This evidence concerns the gene KLHL41 and nemaline myopathy.