Novel gene mutation in von Hippel-Lindau disease – a report of two cases

BACKGROUND: Von Hippel-Lindau (VHL) syndrome is a familial autosomal dominant hereditary neoplastic disease caused by mutations in the VHL gene. Approximately 503 kinds of VHL gene mutations have been reported. Different types of mutations manifest various clinical phenotypes, from benign to maligna...

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Detalles Bibliográficos
Autores principales: Wang, Jitian, Cao, Wenjie, Wang, Zhaoxia, Zhu, Hong
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2019
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6902464/
https://www.ncbi.nlm.nih.gov/pubmed/31823746
http://dx.doi.org/10.1186/s12881-019-0930-8

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