Karlsson Torbjörn, and 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 123, no. 3 (September 25, 2018): 153–157. Accessed November 30, 2024. https://ujms.net/index.php/ujms/article/view/5802.