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

Yasir Sharif | Zendy; Saba Irshad | Zendy; Anam Tariq | Zendy; Sana Rasheed | Zendy; Muhammad Hamza Tariq | Zendy

Open Access

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

Author(s) -

Yasir Sharif,

Saba Irshad,

Anam Tariq,

Sana Rasheed,

Muhammad Hamza Tariq

Publication year - 2019

Publication title -

saudi medical journal

Language(s) - English

Resource type - Journals

SCImago Journal Rank - 0.437

H-Index - 51

eISSN - 1658-3175

pISSN - 0379-5284

DOI - 10.15537/smj.2019.9.24482

Subject(s) - hemochromatosis , hereditary hemochromatosis , medicine , ferritin , mutation , thalassemia , gene mutation , gastroenterology , polymorphism (computer science) , restriction fragment length polymorphism , beta thalassemia , compound heterozygosity , genetics , endocrinology , gene , polymerase chain reaction , genotype , biology

To evaluate any association between the frequency of hereditary hemochromatosis (HFE) gene mutation (H63D and C282Y) and iron overload in beta-thalassemia major (BTM) patients.

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