Source: Molecular Syndromology. Unidade: FM
Subjects: DOENÇAS RARAS, MIOCARDIOPATIA CONGESTIVA
ABNT
LINNENKAMP, Bianca Domit Werner et al. Coexistence of rare genetic disorders in a consanguineous family: case study of KLHL24-related hypertrophic cardiomyopathy and Char Syndrome. Molecular Syndromology, v. 16, n. 2, p. 194-200, 2025Tradução . . Disponível em: https://observatorio.fm.usp.br/handle/OPI/87118. Acesso em: 26 abr. 2026.APA
Linnenkamp, B. D. W., Pires, L. V. L., Stephan, B. de O., Vilalva, K. H., Carvalho, M. L. P. de, Lipari, L. F. V. P., et al. (2025). Coexistence of rare genetic disorders in a consanguineous family: case study of KLHL24-related hypertrophic cardiomyopathy and Char Syndrome. Molecular Syndromology, 16( 2), 194-200. doi:10.1159/000540786NLM
Linnenkamp BDW, Pires LVL, Stephan B de O, Vilalva KH, Carvalho MLP de, Lipari LFVP, Fernandes F, Krieger JE. Coexistence of rare genetic disorders in a consanguineous family: case study of KLHL24-related hypertrophic cardiomyopathy and Char Syndrome [Internet]. Molecular Syndromology. 2025 ; 16( 2): 194-200.[citado 2026 abr. 26 ] Available from: https://observatorio.fm.usp.br/handle/OPI/87118Vancouver
Linnenkamp BDW, Pires LVL, Stephan B de O, Vilalva KH, Carvalho MLP de, Lipari LFVP, Fernandes F, Krieger JE. Coexistence of rare genetic disorders in a consanguineous family: case study of KLHL24-related hypertrophic cardiomyopathy and Char Syndrome [Internet]. Molecular Syndromology. 2025 ; 16( 2): 194-200.[citado 2026 abr. 26 ] Available from: https://observatorio.fm.usp.br/handle/OPI/87118

