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

• Asıl Yazarlar: Jitian Wang (Yazar), Wenjie Cao (Yazar), Zhaoxia Wang (Yazar), Hong Zhu (Yazar)
• Materyal Türü: Kitap
• Baskı/Yayın Bilgisi: BMC, 2019-12-01T00:00:00Z.
• Konular: article
• Online Erişim: Connect to this object online.

Abstract Background 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 types of mutations manifest various clinical phenotypes, from benign to...