Hepcidin and HFE Polymorphisms and Ferritin Level in β-Thalassemia Major

International Journal of Hematology-Oncology and Stem Cell Research

Seyyed Abdolhossein Tavallai Zavareh¹  Fahimeh Moradi²  Negar Asle Rasouli³  Hossein Teimori⁴  Maryam Hosseinpour⁵  Milad Jalil⁶  Kiavash Fekri⁷ 

[1]Department of Pediatrics, Faculty of Medicine, Shahrekord University of Medical Sciences, Shahrekord, Iran

[2]Human Genetics, Cellular and Molecular Research Center, Basic Health Sciences Institute, Shahrekord University of Medical Sciences, Shahrekord, Iran

[3]Medical Biotechnology, Cellular and Molecular Research Center, Basic Health Sciences Institute, Shahrekord University of Medical Sciences, Shahrekord, Iran

[4]Medical Genetics, Cellular and Molecular Research Center, Basic Health Sciences Institute, Shahrekord University of Medical Sciences, Shahrekord, Iran

[5]Molecular Genetics, Cellular and Molecular Research Center, Basic Health Sciences Institute, Shahrekord University of Medical Sciences, Shahrekord, Iran

[6]Molecular Genetics, Tehran Medical Branch, Islamic Azad University, Tehran, Iran

[7]Pediatric Hematology and Oncology, Hajar Hospital Clinical Research Center, Shahrekord University of Medical Sciences, Shahrekord, Iran

关键词: Ferritin;    Hepcidin;    HFE;    Iron overload;    Thalassemia;   

DOI  :  10.18502/ijhoscr.v13i1.324

来源: DOAJ

【 授权许可】

Unknown