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A Review of Von Hippel-Lindau Syndrome
Von Hippel-Lindau syndrome (VHL) is a familial neoplastic condition seen in approximately 1 in 36,000 live births. It is caused by germline mutations of the tumor suppressor gene VHL, located on the short arm of chromosome 3. While the majority of the affected individuals have a positive family hist...
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| Publicado en: | J Kidney Cancer VHL |
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| Autores principales: | , , , , , |
| Formato: | Artigo |
| Lenguaje: | Inglês |
| Publicado: |
Codon Publications
2017
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| Materias: | |
| Acceso en línea: | https://ncbi.nlm.nih.gov/pmc/articles/PMC5541202/ https://ncbi.nlm.nih.gov/pubmed/28785532 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.15586/jkcvhl.2017.88 |
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