Germline mutations in the VHL gene associated with 3 different renal lesions in a Chinese von Hippel-Lindau disease family

Von Hippel–Lindau (VHL) disease is a rare autosomal dominant inherited cancer syndrome that is characterized by hemangioblastomas in the central nervous system and retina, renal cell carcinoma and cysts, pancreatic tumors and cysts, and pheochromocytoma. The underlying gene in this disease is the VH...

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Publicado en:Cancer Biol Ther
Autores principales: Yuan, Ping, Sun, Qipeng, Liang, Hao, Wang, Wenjun, Li, Ling, Wang, Ye, Deng, Huan, Lai, Luhua, Chen, Xiaoli, Zhou, Xiangfu
Formato: Artigo
Lenguaje:Inglês
Publicado: Taylor & Francis 2016
Materias:
Bedside to Bench Report
Acceso en línea:https://ncbi.nlm.nih.gov/pmc/articles/PMC4990403/
https://ncbi.nlm.nih.gov/pubmed/27057652
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1080/15384047.2016.1167293
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