Novel gene mutation in von Hippel-Lindau disease – a report of two cases

Von Hippel-Lindau (VHL) syndrome is a familial autosomal dominant hereditary neoplastic disease caused by mutations in the VHL gene. Approximately 503 kinds of VHL gene mutations have been reported. Different ...

Source: BMC Medical Genetics - December 10, 2019 Category: Genetics & Stem Cells Authors: Jitian Wang, Wenjie Cao, Zhaoxia Wang and Hong Zhu Tags: Case report Source Type: research