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...

Descripció completa

Guardat en:
Dades bibliogràfiques
Publicat a:J Kidney Cancer VHL
Autors principals: Varshney, Neha, Kebede, Amanuel A., Owusu-Dapaah, Harry, Lather, Jason, Kaushik, Manu, Bhullar, Jasneet S.
Format: Artigo
Idioma:Inglês
Publicat: Codon Publications 2017
Matèries:
Review Article
Accés en línia: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
Etiquetes: Afegir etiqueta
Sense etiquetes, Sigues el primer a etiquetar aquest registre!

Ítems similars