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The von Hippel-Lindau Gene: Turning Discovery Into Therapy
Mutations or aberrations of the von Hippel-Lindau gene are responsible for the hereditary neoplastic syndrome that bears the same name, as well as for the majority of sporadic clear cell renal cell carcinomas. The discovery of this gene and subsequent clarification of its mechanism of action have le...
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| Hoofdauteurs: | , |
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| Formaat: | Artigo |
| Taal: | Inglês |
| Gepubliceerd in: |
2008
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| Onderwerpen: | |
| Online toegang: | https://ncbi.nlm.nih.gov/pmc/articles/PMC2963103/ https://ncbi.nlm.nih.gov/pubmed/18800388 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1002/cncr.23645 |
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