Somatic mutations in arteriovenous malformations in hereditary hemorrhagic telangiectasia support a bi-allelic two-hit mutation mechanism of pathogenesis.

• Tác giả: Gonzalo Sapisochin Cantis, Evon DeBose-Scarlett, Marie E Faughnan, Cassi Friday, Carol J Gallione, James R Gossage, Helen Kim, Douglas A Marchuk, Andrew K Ressler, Katharina Schimmel, Edda Spiekerkoetter, Shantel Weinsheimer
• Ngôn ngữ: eng
• Thông tin xuất bản: United States : American journal of human genetics , 2025
• Bộ sưu tập: NCBI
• ID: 718508