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Research ArticleOriginal Article
Open Access

Association of frequency of hereditary hemochromatosis (HFE) gene mutations (H63D and C282Y) with iron overload in beta-thalassemia major patients in Pakistan

Yasir Sharif, Saba Irshad, Anam Tariq, Sana Rasheed and Muhammad H. Tariq
Saudi Medical Journal September 2019, 40 (9) 887-892; DOI: https://doi.org/10.15537/smj.2019.9.24482
Yasir Sharif
From the Institute of Biochemistry and Biotechnology, University of The Punjab, Lahore, Pakistan
MS
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  • For correspondence: [email protected]
Saba Irshad
From the Institute of Biochemistry and Biotechnology, University of The Punjab, Lahore, Pakistan
MS, PhD
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Anam Tariq
From the Institute of Biochemistry and Biotechnology, University of The Punjab, Lahore, Pakistan
BS, MS
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Sana Rasheed
From the Institute of Biochemistry and Biotechnology, University of The Punjab, Lahore, Pakistan
BS, MS
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Muhammad H. Tariq
From the Institute of Biochemistry and Biotechnology, University of The Punjab, Lahore, Pakistan
BS, MS
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Article Information

vol. 40 no. 9 887-892
DOI 
https://doi.org/10.15537/smj.2019.9.24482
PubMed 
31522215

Published By 
Saudi Medical Journal
Online ISSN 
1658-3175
History 
  • Received May 8, 2019
  • Accepted August 8, 2019
  • Published online September 1, 2019.

Copyright & Usage 
Copyright: © Saudi Medical Journal This is an open-access article distributed under the terms of the Creative Commons Attribution-Noncommercial-Share Alike 3.0 Unported, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.

Author Information

  1. Yasir Sharif, MS⇑,
  2. Saba Irshad, MS, PhD,
  3. Anam Tariq, BS, MS,
  4. Sana Rasheed, BS, MS and
  5. Muhammad H. Tariq, BS, MS
  1. From the Institute of Biochemistry and Biotechnology, University of The Punjab, Lahore, Pakistan
  1. Address correspondence and reprint request to: Yasir Sharif, Institute of Biochemistry and Biotechnology, University of the Punjab, Lahore, Pakistan. E-mail: s.yashel36{at}hotmail.com ORCID ID: https://orcid.org/0000-0003-0387-5534
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Cited By...

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This article has been cited by the following articles in journals that are participating in Crossref Cited-by Linking.

  • Comparison between H63D and G71D gene mutation effects on iron overload in Iraqi patients with β-thalassemia major: A case–control study
    SamarAdnan Maatooq, MaysemMouayad Alwash, AbeerAnwer Ahmed
    Iraqi Journal of Hematology 2022 11 1
  • Genetic Correlation of HBB, HFE and HAMP Genes to Endocrinal Complications in Egyptian Beta Thalassemia Major Patients
    Mona F. Sokkar, Mona Hamdy, Mohamed B. Taher, Heba El-Sayed, Eman Abdelmotaleb Bayomi, Khalda S. Amr, Ghada Y. El-Kamah
    Biochemical Genetics 2024
  • The Exploring of Growth Differentiation Factor-15 and H63D Gene Polymorphisms in β-thalassemia Major: Implications for Cardiovascular Risk and Iron Overload
    Hussein Yaqoub Hamza, Ahmed Ghdhban Al-Ziaydi, Aalan Hadi Hassan Alzamili
    Journal of Applied Hematology 2024 15 1
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Saudi Medical Journal: 40 (9)
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Association of frequency of hereditary hemochromatosis (HFE) gene mutations (H63D and C282Y) with iron overload in beta-thalassemia major patients in Pakistan
Yasir Sharif, Saba Irshad, Anam Tariq, Sana Rasheed, Muhammad H. Tariq
Saudi Medical Journal Sep 2019, 40 (9) 887-892; DOI: 10.15537/smj.2019.9.24482

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Association of frequency of hereditary hemochromatosis (HFE) gene mutations (H63D and C282Y) with iron overload in beta-thalassemia major patients in Pakistan
Yasir Sharif, Saba Irshad, Anam Tariq, Sana Rasheed, Muhammad H. Tariq
Saudi Medical Journal Sep 2019, 40 (9) 887-892; DOI: 10.15537/smj.2019.9.24482
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© 2025 Saudi Medical Journal Saudi Medical Journal is copyright under the Berne Convention and the International Copyright Convention.  Saudi Medical Journal is an Open Access journal and articles published are distributed under the terms of the Creative Commons Attribution-NonCommercial License (CC BY-NC). Readers may copy, distribute, and display the work for non-commercial purposes with the proper citation of the original work. Electronic ISSN 1658-3175. Print ISSN 0379-5284.

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