Associated Papers
Recurrent somatic copy number alterations in resected cerebral cavernous malformations.
Ressler AK et al.
Human Genomics, 2025
41366709 (PubMed )
Supplement: 40246_2025_886_MOESM1_ESM.xlsx › Extended_Data_Table_4
Somatic Mutations in Vascular Malformations of Hereditary Hemorrhagic Telangiectasia Result in Bi-allelic Loss of ENG or ACVRL1.
Snellings DA et al.
American Journal of Human Genetics, 2019
Highlights of the 13th International Hereditary Hemorrhagic Telangiectasia Scientific conference.
Choi H et al.
Angiogenesis, 2019
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