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...

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Bibliografske podrobnosti
izdano v:J Kidney Cancer VHL
Main Authors: Varshney, Neha, Kebede, Amanuel A., Owusu-Dapaah, Harry, Lather, Jason, Kaushik, Manu, Bhullar, Jasneet S.
Format: Artigo
Jezik:Inglês
Izdano: Codon Publications 2017
Teme:
Review Article
Online dostop: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
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