DeBose-Scarlett, Evon
Ressler, Andrew K.
Gallione, Carol J.
Sapisochin Cantis, Gonzalo
Friday, Cassi
Weinsheimer, Shantel
Schimmel, Katharina
Spiekerkoetter, Edda
Kim, Helen
Gossage, James R.
Faughnan, Marie E.
Marchuk, Douglas A. https://orcid.org/0000-0002-3110-6671
Funding for this research was provided by:
American Heart Association Inc (23CDA1046402)
National Heart, Lung, and Blood Institute (R01HL169787)
National Institutes of Health (5U54-NS065705)
US Department of Defense (DOD W81XWH-16-PRMRP-FPA)
Fondation Leducq (17 CVD 03)
Fondation Leducq (5U54-NS065705)
Rare Diseases Clinical Research Network
Helen Hamlyn Trust
This article is maintained by: Elsevier
Article Title: Somatic mutations in arteriovenous malformations in hereditary hemorrhagic telangiectasia support a bi-allelic two-hit mutation mechanism of pathogenesis
Journal Title: The American Journal of Human Genetics
CrossRef DOI link to publisher maintained version: https://doi.org/10.1016/j.ajhg.2024.08.020
Content Type: article
Copyright: © 2024 Published by Elsevier Inc. on behalf of American Society of Human Genetics.