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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Detalles Bibliográficos
Autores principales: Varshney, Neha, Kebede, Amanuel A., Owusu-Dapaah, Harry, Lather, Jason, Kaushik, Manu, Bhullar, Jasneet S.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Codon Publications 2017
Materias:
Review Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5541202/
https://www.ncbi.nlm.nih.gov/pubmed/28785532
http://dx.doi.org/10.15586/jkcvhl.2017.88

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5541202/
https://www.ncbi.nlm.nih.gov/pubmed/28785532
http://dx.doi.org/10.15586/jkcvhl.2017.88

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