Two new mutations in the HIF2A gene associated with erythrocytosis-Reference-Cited by-同舟云学术

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Two new mutations in the HIF2A gene associated with erythrocytosis

Published:2012-02-24 Issue:4 Volume:87 Page:439-442
ISSN:0361-8609
Container-title:American Journal of Hematology
language:en
Short-container-title:Am. J. Hematol.

Author:

Percy Melanie J.,Chung Yu Jin,Harrison Claire,Mercieca Jane,Hoffbrand A. Victor,Dinardo Carla L.,Santos Paulo C.J.L.,Fonseca Guilherme H.H.,Gualandro Sandra F.M.,Pereira Alexandre C.,Lappin Terence R.J.,McMullin Mary Frances,Lee Frank S.

Publisher

Wiley

Subject

Hematology

Link

http://onlinelibrary.wiley.com/wol1/doi/10.1002/ajh.23123/fullpdf

Cited by 37 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. Deficiency in PHD2-mediated hydroxylation of HIF2α underlies Pacak-Zhuang syndrome;Communications Biology;2024-02-28

2. Idiopathic erythrocytosis: a germline disease?;Clinical and Experimental Medicine;2024-01-20

3. Comprehensive in silico and functional studies for classification of EPAS1/HIF2A genetic variants identified in patients with erythrocytosis;Haematologica;2023-01-26

4. Clinicopathological characteristics of high-altitude polycythemia-related kidney disease in Tibetan inhabitants;Kidney International;2022-07

5. Erythrocytosis associated with EPAS1(HIF2A), EGLN1(PHD2), VHL, EPOR or BPGM mutations: The Mayo Clinic experience;Haematologica;2022-02-10

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