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Discovering a novel genetic variant in 11 family members who had isolated pheochromocytoma linked to von Hippel-Lindau (VHL) syndrome, aligning with the type 2c phenotype.
Alhawari H, Obeidat Z, Wahbeh L, Mismar A, Younis N, Jafar H, Momani M, Alsabatin N, Awidi A, Alhawari H. Alhawari H, et al. Among authors: obeidat z. Blood Press. 2024 Dec;33(1):2355268. doi: 10.1080/08037051.2024.2355268. Epub 2024 Jun 2. Blood Press. 2024. PMID: 38824681 Free article.