Study of the effect of HFE gene mutations on iron overload in Egyptian thalassemia patients-Reference-Cited by-同舟云学术

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Study of the effect of HFE gene mutations on iron overload in Egyptian thalassemia patients

Published:2015-04 Issue:2 Volume:16 Page:129-133
ISSN:1110-8630
Container-title:Egyptian Journal of Medical Human Genetics
language:en
Short-container-title:Egyptian Journal of Medical Human Genetics

Author:

Wilson Manal Michel,Al-Wakeel Hanan,Said Fadwa,El-Ghamrawy Mona,Assaad Mary,El-Beshlawy Amal

Publisher

Springer Science and Business Media LLC

Subject

Genetics (clinical)

Reference38 articles.

1. Beta thalassemia;Galanello;Orphanet J Rare Dis,2010

2. Prevention of hemoglobinopathies in Egypt;El-Beshlawy;Hemoglobin,2009

3. Screening for beta-thalassaemia carriers in Egypt: significance of the osmotic fragility test;El-Beshlawy;East Mediterr Health J,2007

4. Hepcidin in beta-thalassemia;Nemeth;Ann N Y Acad Sci,2010

5. Disorders of hemoglobin: genetics, pathophysiology and clinical management;Steinberg,2009

Cited by 5 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. Genetic Correlation of HBB, HFE and HAMP Genes to Endocrinal Complications in Egyptian Beta Thalassemia Major Patients;Biochemical Genetics;2024-07-02

2. The Exploring of Growth Differentiation Factor-15 and H63D Gene Polymorphisms in β-thalassemia Major: Implications for Cardiovascular Risk and Iron Overload;Journal of Applied Hematology;2024-01

3. Frequency of hereditary hemochromatosis gene mutations and their effects on iron overload among beta thalassemia patients of Chennai residents;AIMS Molecular Science;2021

4. Hemochromatosis in a β‐thalassemia minor patient with H63D homozygous mutation: A case report;Clinical Case Reports;2020-07-12

5. Investigation of correlation between H63D and C282Y mutations in HFE gene and serum Ferritin level in beta-thalassemia major patients;Transfusion Clinique et Biologique;2019-11

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