Genetic basis of unexplained erythrocytosis in Indian patients

Author:

Mallik Nabhajit1,Sharma Prashant1ORCID,Kaur Hira Jasbir1,Chhabra Sanjeev1,Sreedharanunni Sreejesh1,Kumar Narender1,Naseem Shano1,Sachdeva Man Updesh Singh1,Ahluwalia Jasmina1,Malhotra Pankaj2,Varma Neelam1,Varma Subhash2,Das Reena1ORCID

Affiliation:

1. Department of Hematology Postgraduate Institute of Medical Education and Research Chandigarh India

2. Department of Internal Medicine Postgraduate Institute of Medical Education and Research Chandigarh India

Publisher

Wiley

Subject

Hematology,General Medicine

Cited by 16 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. Wide spectrum of novel and rare hemoglobin variants in the multi‐ethnic Indian population: A review;International Journal of Laboratory Hematology;2024-03-19

2. Coexistence of multiple gene variants in some patients with erythrocytoses;Mediterranean Journal of Hematology and Infectious Diseases;2024-02-29

3. Whole Exome Sequencing Reveals Novel Variants in Unexplained Erythrocytosis;OMICS: A Journal of Integrative Biology;2023-07-01

4. A Screening Approach for Inherited Erythrocytosis due to the VHL:c.598C > T Mutation (Chuvash Polycythemia);Indian Journal of Hematology and Blood Transfusion;2023-05-14

5. Incidence of ancient variants associated with oncological diseases in modern populations;Biotechnology & Biotechnological Equipment;2023-01-09

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