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Erythrocytosis associated with EPAS1(HIF2A), EGLN1(PHD2), VHL, EPOR or BPGM mutations: The Mayo Clinic experience.

Haematologica - 1 May 2022

Gangat Naseema, Oliveira Jennifer L, Porter Tavanna R, Hoyer James D, Al-Kali Aref, Patnaik Mrinal M, Pardanani Animesh, Tefferi Ayalew

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PMID: 35142155
DOI: 10.3324/haematol.2021.280516
PMCID: PMC9052925

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Erythrocytosis associated with EPAS1(HIF2A), EGLN1(PHD2), VHL, EPOR or BPGM mutations: The Mayo Clinic experience.PMID 35142155Read ↗

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Characterization of genetic variants in the EGLN1/PHD2 gene identified in a European collection of patients with erythrocytosisSemantic proximity Read ↗

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