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A Case of von Hippel–Lindau Disease with Colorectal Adenocarcinoma, Renal Cell Carcinoma and Hemangioblastomas

von Hippel–Lindau (VHL) disease is an autosomal dominant inherited tumor syndrome associated with mutations of the VHL tumor suppressor gene located on chromosome 3p25. The loss of functional VHL protein contributes to tumorigenesis. This condition is characterized by development of benign and malig...

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Dettagli Bibliografici
Pubblicato in:Cancer Res Treat
Autori principali: Heo, Su Jin, Lee, Choong-kun, Hahn, Kyu Yeon, Kim, Gyuri, Hur, Hyuk, Choi, Sung Hoon, Han, Kyung Seok, Cho, Arthur, Jung, Minkyu
Natura: Artigo
Lingua:Inglês
Pubblicazione: Korean Cancer Association 2016
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Accesso online:https://ncbi.nlm.nih.gov/pmc/articles/PMC4720105/
https://ncbi.nlm.nih.gov/pubmed/25715769
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.4143/crt.2014.299
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