Gene List:
BIN1, CCDC78, DNM2, MTM1, MYF6, RYR1, SPEG, TTN

References:
Schnitzler LJ, et al. Sporadic late-onset nemaline myopathy: clinico-pathological characteristics and review of 76 cases. Orphanet J Rare Dis. 2017 May 11;12(1):86.

Savarese M, et al. Increasing Rold of Titin Mutations in Neuromuscular Disorders. J Neuromuscul Dis. 2016;3(3):293-308.