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Acute myeloid leukemia in a 38-year-old hemodialyzed patient with von Hippel-Lindau disease
Von Hippel-Lindau disease (VHL disease) is a hereditary cancer predisposition syndrome caused by mutations of the von Hippel-Lindau tumor suppressor gene. The gene product, pVHL, regulates the level of proteins that play a central role in protecting cells against hypoxia. Clinical hallmarks of von H...
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| Auteurs principaux: | , , , , |
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| Format: | Artigo |
| Langue: | Inglês |
| Publié: |
BioMed Central
2013
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| Sujets: | |
| Accès en ligne: | https://ncbi.nlm.nih.gov/pmc/articles/PMC3846582/ https://ncbi.nlm.nih.gov/pubmed/23968328 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/1897-4287-11-11 |
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