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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Kaydedildi:
Detaylı Bibliyografya
Yayımlandı:J Kidney Cancer VHL
Asıl Yazarlar: Varshney, Neha, Kebede, Amanuel A., Owusu-Dapaah, Harry, Lather, Jason, Kaushik, Manu, Bhullar, Jasneet S.
Materyal Türü: Artigo
Dil:Inglês
Baskı/Yayın Bilgisi: Codon Publications 2017
Konular:
Review Article
Online Erişim: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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