Genetic heterogeneity of primary familial and congenital polycythemia
Author:
Publisher
Wiley
Subject
Hematology
Reference26 articles.
1. Autosomal dominant polycythemia
2. Familial and congenital polycythemia in three unrelated families
3. Truncated erythropoietin receptor causes dominantly inherited benign human erythrocytosis.
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1. Elevated erythroferrone distinguishes erythrocytosis with inherited defects in oxygen‐sensing pathway from primary familial and congenital polycythaemia;British Journal of Haematology;2023-05-28
2. Identification of Two Novel EPOR Gene Variants in Primary Familial Polycythemia: Case Report and Literature Review;Genes;2022-09-20
3. Effects of idiopathic erythrocytosis on the left ventricular diastolic functions and the spectrum of genetic mutations: A case control study;Medicine;2022-08-12
4. Novel mutations in EPO-R and oxygen-dependent degradation (ODD) domain of EPAS1 genes-a causative reason for Congenital Erythrocytosis;European Journal of Medical Genetics;2022-06
5. Clinical Characteristics of Pediatric Patients with Congenital Erythrocytosis: A Single-Center Study;Indian Journal of Hematology and Blood Transfusion;2021-08-25
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