DeBose-Scarlett, E., Ressler, A. K., Gallione, C. J., Cantis, G. S., Friday, C., Weinsheimer, S., … Marchuk, D. A. (2025). Somatic mutations in arteriovenous malformations in hereditary hemorrhagic telangiectasia support a bi-allelic two-hit mutation mechanism of pathogenesis. Am J Hum Genet, 112(4), 963. https://doi.org/10.1016/j.ajhg.2025.03.007

DeBose-Scarlett, Evon, Andrew K. Ressler, Carol J. Gallione, Gonzalo Sapisochin Cantis, Cassi Friday, Shantel Weinsheimer, Katharina Schimmel, et al. “Somatic mutations in arteriovenous malformations in hereditary hemorrhagic telangiectasia support a bi-allelic two-hit mutation mechanism of pathogenesis.” Am J Hum Genet 112, no. 4 (April 3, 2025): 963. https://doi.org/10.1016/j.ajhg.2025.03.007.

DeBose-Scarlett E, Ressler AK, Gallione CJ, Cantis GS, Friday C, Weinsheimer S, et al. Somatic mutations in arteriovenous malformations in hereditary hemorrhagic telangiectasia support a bi-allelic two-hit mutation mechanism of pathogenesis. Am J Hum Genet. 2025 Apr 3;112(4):963.

DeBose-Scarlett, Evon, et al. “Somatic mutations in arteriovenous malformations in hereditary hemorrhagic telangiectasia support a bi-allelic two-hit mutation mechanism of pathogenesis.” Am J Hum Genet, vol. 112, no. 4, Apr. 2025, p. 963. Pubmed, doi:10.1016/j.ajhg.2025.03.007.

DeBose-Scarlett E, Ressler AK, Gallione CJ, Cantis GS, Friday C, Weinsheimer S, Schimmel K, Spiekerkoetter E, Kim H, Gossage JR, Faughnan ME, Marchuk DA. Somatic mutations in arteriovenous malformations in hereditary hemorrhagic telangiectasia support a bi-allelic two-hit mutation mechanism of pathogenesis. Am J Hum Genet. 2025 Apr 3;112(4):963.