Genetic origins and clinical phenotype of familial and acquired erythrocytosis and thrombocytosis
Author:
Publisher
Wiley
Subject
Hematology
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1. Analysis of mutations in EPOR, VHL, EPAS1 and EGLN1 genes associated with the familial erythrocytosis ECYT1-4 among JAK2- and CALR-negative patients with the erythrocytosis of unclear etiology;Russian journal of hematology and transfusiology;2023-12-28
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5. Receptors | Hematopoietin Receptors;Encyclopedia of Biological Chemistry III;2021
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