Identification of novel MYO19 variants in neonatal hypertrophic cardiomyopathy: a familial analysis revealing oligogenic contributors to disease severity. - Cho HW; Kim H; Kim JM; Shin DM; Kim OH; Yang M; Jo HS; Jang MA; Jang JH; Park HY; Chang YS; Park MH (Orphanet journal of rare diseases, 2025)