Gene List:
ACTA1, BIN1, CCDC78, CCDC78, CFL2, CFL2, CHKB, CNTN1, COL12A1, COL6A1, COL6A2, COL6A3, DNM2, KBTBD13, KLHL40, KLHL41, LMOD3, MEGF10, MTM1, MYF6, MYH2, MYH7, NEB, RYR1, SCN4A, SELENON, SEPN1, SPEG, STAC3, TNNT1, TPM2, TPM3, TTN

References:
Kuhn M, et al. Utility of a next-generation sequencing-based gene panel investigation in German patients with genetically unclassified limb-girdle muscular dystrophy. J Neurol 263, 743–750 (2016).

Kress W, et al. The Genetic Approach: Next-Generation Sequencing-Based Diagnosis of Congenital and Infantile Myopathies/Muscle Dystrophies. Neuropediatrics 2017; 48(04): 242-246.

Cassandrini D, et al. Congenital Myopathies: clinical phenotypes and new diagnostic tools. Ital J Pediatr. 2017 Nov 15;43(1):101.