Gene List:
ACTA1, BIN1, CFL2, KBTBD13, KLHL40, KLHL41, LMOD3, MTM1, MYPN, NEB, TNNT1, TPM2, TPM3

References:
Ryan MM, et al. Nemaline myopathy: a clinical study of 143 cases. Ann Neurol. 2001 Sep;50(3):312-20.

Ong et al. Novel cofilin-2 (CFL2) four base pair deletion causing nemaline myopathy. J Neurol Neurosurg Psychiatry. 2014;85:1058–60.

North K.N. and Ryan M.M. Nemaline Myopathy. Pagon RA, Adam MP, Ardinger HH, et al., editors. Seattle (WA): University of Washington, Seattle; 1993-2017.

Anderson et al. Nemaline myopathy in the Ashkenazi Jewish population is caused by a deletion in the nebulin gene. Hum Genet. 2004;115:185–90.

Donner et al. Mutations in the beta-tropomyosin (TPM2) gene–a rare cause of nemaline myopathy. Neuromuscul Disord. 2002;12:151–8.

Lehtokari VL, et al. Mutation update: the spectra of nebulin variants and associated myopathies. Hum Mutat. 2014 Dec;35(12):1418-26.