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Novel three missense mutations observed in Von Hippel-Lindau gene in a patient reported with renal cell carcinoma
Von Hippel-Lindau (VHL) disease is an autosomal dominant hereditary cancer syndrome that predisposes to the development of a variety of benign and malignant tumors, especially cerebellar hemangioblastomas, retinal angiomas and clear-cell renal cell carcinomas (RCC). We have identified of VHL gene us...
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| Main Authors: | , , , , , , |
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| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
Medknow Publications & Media Pvt Ltd
2013
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC3841571/ https://ncbi.nlm.nih.gov/pubmed/24339559 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.4103/0971-6866.120809 |
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