Gene List:
ACTA1, AGL, AMPD1, ANO5, ATP2A1, B3GALNT2, B4GAT1, BAG3, BICD2, BIN1, BSCL2, BVES, CACNA1S, CAPN3, CAV3, CAVIN1, CCDC78, CFL2, CHAT, CHKB, CHRNA1, CHRNB1, CHRND, CHRNE, CHRNG, CLCN1, CNTN1, COL12A1, COL6A1, COL6A2, COL6A3, COLQ, CRPPA, CRYAB, DAG1, DES, DMD, DNAJB6, DNM2, DOK7, DPM1, DPM2, DPM3, DYNC1H1, DYSF, EMD, FHL1, FKRP, FKTN, FLNC, GAA, GBE1, GLE1, GMPPB, GNE, HNRNPDL, IGHMBP2, ISPD, ITGA7, KBTBD13, KLHL40, KLHL41, LAMA2, LAMP2, LARGE1, LDB3, LIMS2, LMNA, LMOD3, MATR3, MEGF10, MICU1, MTM1, MTMR14, MUSK, MYH2, MYH7, MYOT, NEB, PABPN1, PFKM, PHKA1, PLEC, PLEKHG5, PMM2, PNPLA2, POLG, POLG2, POMGNT1, POMGNT2, POMK, POMT1, POMT2, PYGM, RAPSN, RRM2B, RXYLT1, RYR1, SCN4A, SELENON, SGCA, SGCB, SGCD, SGCE, SGCG, SIL1, SMCHD1, SPEG, STAC3, SUCLA2, SYNE1, SYNE2, TCAP, TIA1, TK2, TMEM43, TNNI2, TNNT1, TNPO3, TOR1AIP1, TPM2, TPM3, TRAPPC11, TRIM32, TRIP4, TRPV4, TTN, TWNK, TYMP, UBA1, VCP, VRK1

References:
Gonzalez-Quereda, L. et al. Two different NGS approaches to address molecular diagnosis of congenital neuromuscular diseases. Neuromuscular Disorders. 2017; 27(2):S197.

Teoh HL, et al. Approaches to genetic diagnosis in neuromuscular conditions in the era of next generation sequencing. Journal of Neurology, Neurosurgery & Psychiatry 2016;87:1384-1385.