[A case of familial erythrocytosis type 2 caused by VHL gene mutation]

Zhonghua Xue Ye Xue Za Zhi. 2020 Dec 14;41(12):1047-1049. doi: 10.3760/cma.j.issn.0253-2727.2020.12.015.

[Article in Chinese]

Authors

W Zhang¹, S Bao¹, L J Jiang², Y P Ma¹

Affiliations

¹ Department of Hematology, People's Hospital of Ningxia Hui Autonomous Region, Yinchuan 750021, China.
² Ningxia Geriatric Center, People's Hospital of Ningxia Hui Autonomous Region, Yinchuan 750021, China.

PMID: 33445856
PMCID: PMC7840559
DOI: 10.3760/cma.j.issn.0253-2727.2020.12.015

No abstract available

Publication types

Case Reports

MeSH terms

Humans
Mutation
Pedigree
Polycythemia* / congenital
Polycythemia* / genetics
Von Hippel-Lindau Tumor Suppressor Protein / genetics

Substances

Von Hippel-Lindau Tumor Suppressor Protein
VHL protein, human

Supplementary concepts

Polycythemia, primary familial and congenital