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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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Détails bibliographiques
Publié dans:J Kidney Cancer VHL
Auteurs principaux: Varshney, Neha, Kebede, Amanuel A., Owusu-Dapaah, Harry, Lather, Jason, Kaushik, Manu, Bhullar, Jasneet S.
Format: Artigo
Langue:Inglês
Publié: Codon Publications 2017
Sujets:
Accès en ligne: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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