Investigation of correlation between H63D and C282Y mutations in HFE gene and serum Ferritin level in beta-thalassemia major patients

Author:

Rahmani Romina,Naseri Parisa,Safaroghli-Azar Ava,Tarighi Shahriar,hosseini Tahereh,Hojjati Mohammad TaherORCID

Publisher

Elsevier BV

Subject

Biochemistry (medical),Clinical Biochemistry,Hematology

Reference26 articles.

1. Iranian hereditary hemochromatosis patients: baseline characteristics, laboratory data and gene mutations;Zamani;Med Sci Monit,2012

2. Distribution of C282Y and H63D mutations in the HFE gene in healthy Asian Indians and patients with thalassaemia major;Kaur G1;Natl Med J India,2003

3. Analysis of C282Y and H63D mutations of the HFE gene in patients with persistent hyperferritinemia;Leăo;J Med Med Sci,2010

4. Diagnostic value of fructosamine and glycosylated hemoglobin in estimating blood glucose level in diabetic patients with thalassemia major;Kosaryan;mljgoums,2013

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

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