Hemochromatosis in a β‐thalassemia minor patient with H63D homozygous mutation: A case report
Author:
Affiliation:
1. Department of Internal Medicine Tribhuvan University Institute of Medicine Kathmandu Nepal
2. Department of Hemato‐Oncology Tribhuvan University Institute of Medicine Kathmandu Nepal
Publisher
Wiley
Subject
General Medicine
Link
https://onlinelibrary.wiley.com/doi/pdf/10.1002/ccr3.3096
Reference20 articles.
1. Prevalence of Hereditary Hemochromatosis in 16 031 Primary Care Patients
2. Diagnosis and management of hemochromatosis: 2011 Practice Guideline by the American Association for the Study of Liver Diseases
3. The Thalassaemia Syndromes
4. ACG Clinical Guideline: Hereditary Hemochromatosis
5. The Hemochromatosis 845 G→A and 187 C→G Mutations: Prevalence in Non-Caucasian Populations
Cited by 3 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. The Effect of Ferritin Level and Gene Expression of β-globin Promoter with β-thalassemia Patients in Al-Qadisiyah Governorate, Iraq;Journal of Applied Hematology;2023
2. Comparison between H63D and G71D gene mutation effects on iron overload in Iraqi patients with β-thalassemia major: A case–control study;Iraqi Journal of Hematology;2022
3. Rare co-inherited alpha-thalassemia minor and beta-thalassemia minor with heterozygous H63D mutation mistaken as iron deficiency anemia: a case report;AME Case Reports;2022-01
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