Frequent Mutations of VHL Gene and the Clinical Phenotypes in the Largest Chinese Cohort With Von Hippel-Lindau Disease.

Hong, Baoan; Ma, Kaifang; Zhou, Jingcheng; Zhang, Jiufeng; Wang, Jiangyi; Liu, Shengjie; Zhang, Zhongyuan; Cai, Lin; Zhang, Ning; Gong, Kan

Hong, Baoan; Ma, Kaifang; Zhou, Jingcheng; Zhang, Jiufeng; Wang, Jiangyi; Liu, Shengjie; Zhang, Zhongyuan; Cai, Lin; Zhang, Ning; Gong, Kan.

Afiliação

Hong B; Department of Urology, Peking University First Hospital, Beijing, China.
Ma K; Hereditary Kidney Cancer Research Center, Peking University First Hospital, Beijing, China.
Zhou J; Institute of Urology, Peking University, Beijing, China.
Zhang J; National Urological Cancer Center, Beijing, China.
Wang J; Department of Urology, Beijing Cancer Hospital, Beijing, China.
Liu S; Beijing Institute for Cancer Research, Beijing, China.
Zhang Z; Department of Urology, Peking University First Hospital, Beijing, China.
Cai L; Hereditary Kidney Cancer Research Center, Peking University First Hospital, Beijing, China.
Zhang N; Institute of Urology, Peking University, Beijing, China.
Gong K; National Urological Cancer Center, Beijing, China.

Front Genet ; 10: 867, 2019.

Article em En | MEDLINE | ID: mdl-31620170

Palavras-chave

VHL mutation; genotypephenotype correlation; onset age; survival; von HippelLindau disease

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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Tipo de estudo: Risk_factors_studies Idioma: En Revista: Front Genet Ano de publicação: 2019 Tipo de documento: Article

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