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.
Saved in:
| Title: | 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. |
|---|---|
| Authors: | Alhawari, Hussein1 (AUTHOR) h.alhawari@ju.edu.jo, Obeidat, Zaina1 (AUTHOR), Wahbeh, Lina1 (AUTHOR), Mismar, Ayman2 (AUTHOR), Younis, Nedal2 (AUTHOR), Jafar, Hanan1 (AUTHOR), Momani, Munther1 (AUTHOR), Alsabatin, Nedal2 (AUTHOR), Awidi, Abdalla1 (AUTHOR), Alhawari, Hussam1 (AUTHOR) |
| Source: | Blood Pressure. Aug2024, Vol. 33 Issue 1, p1-6. 6p. |
| Database: | Academic Search Ultimate |
|
Full text is not displayed to guests.
Login for full access.
|
|
| ISSN: | 08037051 |
|---|---|
| DOI: | 10.1080/08037051.2024.2355268 |
