The Inactivating biallelic pathogenic sequence variants in the TMOD4 have been associated with myopathy (e.g., nemaline myopathy OMIM #609284) also reported in zebrafish-mutated model (Berger et al., 2014), suggesting that TMOD4 mutations may lead to OSAS relevant myopathy, in the intercostal muscles and/or diaphragm. The gene discussed is TMOD4; the disease is nemaline myopathy.