von Hippel-Lindau Disease: an Update

被引:0
作者
Eamonn R Maher
Richard N Sandford
机构
[1] University of Cambridge,Department of Medical Genetics
[2] NIHR Cambridge Biomedical Research Centre,undefined
[3] Cancer Research UK Cambridge Centre,undefined
来源
Current Genetic Medicine Reports | 2019年 / 7卷
关键词
Inherited; von Hippel-Lindau disease; Phaeochromocytoma; Renal cell carcinoma; Haemangioblastomas; tumour suppressor gene;
D O I
暂无
中图分类号
学科分类号
摘要
引用
收藏
页码:227 / 235
页数:8
相关论文
共 649 条
[1]  
Gossage L(2015)VHL, the story of a tumour suppressor gene NatRev Cancer 15 55-64
[2]  
Eisen T(2016)Von Hippel-Lindau disease: genetics and role of genetic counseling in a multiple neoplasia syndrome J Clin Oncol 34 2172-2181
[3]  
Maher ER(1995)Molecular analysis of de novo germline mutations in the von Hippel-Lindau disease gene Hum Mol Genet 4 2139-2134
[4]  
Nielsen SM(1990)Clinical features and natural history of von Hippel-Lindau disease Q J Med 77 1151-1163
[5]  
Rhodes L(2007)Genotype-phenotype correlations in von Hippel-Lindau disease Hum Mutat 28 143-149
[6]  
Blanco I(2011)von Hippel-Lindau disease: a clinical and scientific review Eur J Hum Genet 19 617-623
[7]  
Chung WK(1993)Identification of the von Hippel-Lindau disease tumor suppressor gene Science (New York, N.Y.) 260 1317-1320
[8]  
Eng C(2016)VHLdb: a database of von Hippel-Lindau protein interactors and mutations Sci Rep 6 31128-62
[9]  
Maher ER(2002)Endemic polycythemia in Russia: mutation in the VHL gene Blood Cells Mol Dis 28 57-1152
[10]  
Richard S(2014)VHL mosaicism can be detected by clinical next-generation sequencing and is not restricted to patients with a mild phenotype Eur J Hum Genet 22 1149-470