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Identification of 3 novel VHL germ-line mutations in Danish VHL patients
BACKGROUND: von Hippel-Lindau (VHL) disease is a hereditary cancer syndrome in which the patients develop retinal and central nervous system hemangioblastomas, pheochromocytomas and clear-cell renal tumors. The autosomal dominant disease is caused by mutations in the VHL gene. METHODS: VHL mutationa...
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Asıl Yazarlar: | , , , , |
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Materyal Türü: | Artigo |
Dil: | Inglês |
Baskı/Yayın Bilgisi: |
BioMed Central
2012
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Konular: | |
Online Erişim: | https://ncbi.nlm.nih.gov/pmc/articles/PMC3458949/ https://ncbi.nlm.nih.gov/pubmed/22799452 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/1471-2350-13-54 |
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