Coexistence of rare genetic disorders in a consanguineous family: case study of KLHL24-related hypertrophic cardiomyopathy and Char Syndrome - Linnenkamp, Bianca Domit Werner; Pires, Lucas Vieira Lacerda; Stephan, Bruno de Oliveira; Vilalva, Kelvin Henrique; Carvalho, Mariana Lombardi Peres de; Lipari, Layara Fernanda Vicente Pereira; Fernandes, Fabio; Krieger, Jose Eduardo (Molecular Syndromology, 2025)