The Role of VHL in the Development of von Hippel-Lindau Disease and Erythrocytosis

Von Hippel-Lindau disease (VHL disease or VHL syndrome) is a familial multisystem neoplastic syndrome stemming from germline disease-associated variants of the <i>VHL</i> tumor suppressor gene on chromosome 3. VHL is involved, through the EPO-VHL-HIF signaling axis, in oxygen sensing and...

Full description

Bibliographic Details
Main Authors: Petra Hudler, Mojca Urbancic
Format: Article
Language:English
Published: MDPI AG 2022-02-01
Series:Genes
Subjects:
Online Access:https://www.mdpi.com/2073-4425/13/2/362