KARLSSON , Torbjörn; CHERIF , Honar. Mutations in the ENG, ACVRL1, and SMAD4 genes and clinical manifestations of hereditary haemorrhagic telangiectasia: experience from the Center for Osler’s Disease, Uppsala University Hospital. Upsala Journal of Medical Sciences, [S. l.], v. 123, n. 3, p. 153–157, 2018. DOI: 10.1080/03009734.2018.1483452. Disponível em: https://ujms.net/index.php/ujms/article/view/5802. Acesso em: 15 nov. 2026.