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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...
Kaydedildi:
| Yayımlandı: | Cancer Biol Ther |
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| Asıl Yazarlar: | , , , , , , , , , |
| Materyal Türü: | Artigo |
| Dil: | Inglês |
| Baskı/Yayın Bilgisi: |
Taylor & Francis
2016
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| Konular: | |
| Online Erişim: | 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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