Inherited haemochromatosis with C282Y mutation in a patient with alpha-thalassaemia: a treatment dilemma

Author:

Al Qasem Mohammed Abdullah,Hanna Fayez,Vithanarachchi Usira S,Khalafallah Alhossain AORCID

Publisher

BMJ

Subject

General Medicine

Reference15 articles.

1. HFE gene mutations in Brazilian thalassemic patients;Oliveira;Braz J Med Biol Res,2006

2. The prevalence and genotypes of alpha-thalassemia in Adiyaman: two rare alpha variants: Adiyaman’da alfa-talasemi genotipleri ve sikligi: Iki nadir alfa variant;Genc;Turk J Biochem,2016

3. Evaluation of Alpha-Thalassemia Mutations in Cases with Hypochromic Microcytic Anemia: The İstanbul Perspective;Karakaş;Turk J Haematol,2015

4. Clinical management of hemochromatosis: current perspectives;Brissot;Int J Clin Transfus Med,2017

5. Detection of α-thalassemia-1 Southeast Asian and Thai type deletions and β-thalassemia 3.5-kb deletion by single-tube multiplex real-time PCR with SYBR Green1 and high-resolution melting analysis;Pornprasert;Korean J Lab Med,2011

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