A Review of Von Hippel-Lindau Syndrome

Von Hippel-Lindau syndrome (VHL) is a familial neoplastic condition seen in approximately 1 in 36,000 live births. It is caused by germline mutations of the tumor suppressor gene VHL, located on the short arm of chromosome 3. While the majority of the affected individuals have a positive family hist...

Полное описание

Сохранить в:
Библиографические подробности
Опубликовано в: :J Kidney Cancer VHL
Главные авторы: Varshney, Neha, Kebede, Amanuel A., Owusu-Dapaah, Harry, Lather, Jason, Kaushik, Manu, Bhullar, Jasneet S.
Формат: Artigo
Язык:Inglês
Опубликовано: Codon Publications 2017
Предметы:
Review Article
Online-ссылка:https://ncbi.nlm.nih.gov/pmc/articles/PMC5541202/
https://ncbi.nlm.nih.gov/pubmed/28785532
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.15586/jkcvhl.2017.88
Метки: Добавить метку
Нет меток, Требуется 1-ая метка записи!

Схожие документы