Genetic analysis of erythrocytosis reveals possible causative and modifier gene mutations
Author:
Affiliation:
1. Department of Biomedicine and Prevention University of Rome Tor Vergata RomeItaly
2. Department of Medicine University of Padua Medical School Padua Italy
Funder
Società Italiana di Ematologia Sperimentale
Publisher
Wiley
Subject
Hematology
Link
https://onlinelibrary.wiley.com/doi/pdf/10.1111/bjh.15931
Reference9 articles.
1. A Knock-in Mouse Model of Human PHD2 Gene-associated Erythrocytosis Establishes a Haploinsufficiency Mechanism
2. HFE mutations in idiopathic erythrocytosis
3. High HFE mutation incidence in idiopathic erythrocytosis
4. The role of PHD2 mutations in the pathogenesis of erythrocytosis
5. PHD2Mutation and Congenital Erythrocytosis with Paraganglioma
Cited by 2 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. Idiopathic erythrocytosis: A diagnostic and management challenge with emerging areas for exploration;British Journal of Haematology;2024-01-23
2. Identification of Variants Associated With Rare Hematological Disorder Erythrocytosis Using Targeted Next-Generation Sequencing Analysis;Frontiers in Genetics;2021-07-19
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