ReviewZhonghua xue ye xue za zhi = Zhonghua xueyexue zazhi2025
[Familial erythrocytosis type 2 due to VHL germline mutations: a case report and literature review].
N N Liu, L J Pan, Z J Xiao, Z F Xu
Abstract readCase ReportsReviewEnglish Abstract
In one paragraphReview in Zhonghua xue ye xue za zhi = Zhonghua xueyexue zazhi, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.
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2 · The registryThe trial behind it
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3 · Its place in the literatureWho cites it
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4 · The recordCorrections and comments
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5 · Who and what moneyAuthors and funding
4 authors.
N N LiuState Key Laboratory of Experimental Hematology, National Clinical Research Center for Blood Diseases, Haihe Laboratory of Cell Ecosystem, Institute of Hematology & Blood Diseases Hospital, Chinese Academy of Medical Sciences & Peking Union Medical College, Tianjin 300020, China Tianjin Institutes of Health Science, Tianjin 301600, China.
L J PanState Key Laboratory of Experimental Hematology, National Clinical Research Center for Blood Diseases, Haihe Laboratory of Cell Ecosystem, Institute of Hematology & Blood Diseases Hospital, Chinese Academy of Medical Sciences & Peking Union Medical College, Tianjin 300020, China Tianjin Institutes of Health Science, Tianjin 301600, China.
Z J XiaoState Key Laboratory of Experimental Hematology, National Clinical Research Center for Blood Diseases, Haihe Laboratory of Cell Ecosystem, Institute of Hematology & Blood Diseases Hospital, Chinese Academy of Medical Sciences & Peking Union Medical College, Tianjin 300020, China Tianjin Institutes of Health Science, Tianjin 301600, China.
Z F XuState Key Laboratory of Experimental Hematology, National Clinical Research Center for Blood Diseases, Haihe Laboratory of Cell Ecosystem, Institute of Hematology & Blood Diseases Hospital, Chinese Academy of Medical Sciences & Peking Union Medical College, Tianjin 300020, China Tianjin Institutes of Health Science, Tianjin 301600, China.
Funding
CAMS Initiative Fund for Medical Sciences 2022-I2M-1-022Clinical research fund from National Clinical Research Centre for Blood Diseases 2023NCRCA0117, 2023NCRCA0103National Natural Science Foundation of China 82170139, 82070134
6 · The paper itselfAbstract
To enhance the understanding of familial erythrocytosis type 2 (ECYT2) resulting from compound heterozygous mutations in the VHL gene.
Indexed as
Germ-Line MutationPolycythemiaVon Hippel-Lindau Tumor Suppressor ProteinAdultHumansMaleRetrospective StudiesVHL protein, humanVon Hippel-Lindau Tumor Suppressor ProteinFamilial erythrocytosis type 2Germline mutationHereditary erythrocytosisVHL gene
Identifiers
PMID40059686
PMCPMC11886440
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