[A Case of Familial Erythrocytosis Type 2 Caused by VHL Gene Mutation]

Overview

Journal Zhonghua Xue Ye Xue Za Zhi

Specialty Hematology

Date 2021 Jan 15

PMID 33445856

Citations 1

Authors

W Zhang

S Bao

L J Jiang

Y P Ma

Affiliations

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Citing Articles

[Familial erythrocytosis type 2 due to VHL germline mutations: a case report and literature review].

Liu N, Pan L, Xiao Z, Xu Z Zhonghua Xue Ye Xue Za Zhi. 2025; 46(1):75-80.

PMID: 40059686 PMC: 11886440. DOI: 10.3760/cma.j.cn121090-20241011-00390.

VHL syndrome without clear family history: A rare case report and literature review of Chinese patients.

Li Y, Xin X, Song W, Zhang X, Chen S, Wang Q Front Neurol. 2022; 13:951054.

PMID: 36324386 PMC: 9618664. DOI: 10.3389/fneur.2022.951054.

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