1.
Karlsson T, Cherif H. 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. ujms [Internet]. 2018Sep.25 [cited 2024Mar.29];123(3):153–157. Available from: https://ujms.net/index.php/ujms/article/view/5802