GENETIC VARIATION IMPACTS IN PATIENTS WITH MAJOR BETA-THALASSEMIA (LETTER TO THE EDITOR)

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NAJAF POUR MALIHEH; FARSHDOUSTI HAGH MAJID; MOVASAGPOOR AKBARI ALI AKBAR; HOSEIN POOR FEYZI ABBAS ALI; MALAKI MAJID

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Journal: Iranian Journal of Public Health Year:2015 | Volume:44 | Issue:5 Page(s): 722-723

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Title

GENETIC VARIATION IMPACTS IN PATIENTS WITH MAJOR BETA-THALASSEMIA (LETTER TO THE EDITOR)

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Abstract

Dear Editor-in-Chief: Thalassemia is the most common single gene disorder around the world. This disease is a type of chronic, microcytic and inherited anemia associated with defect in hemoglobin synthesis and reduction in life span of red blood cells. Thalassemia is distributed in Mediterranean, Middle East, Arabian Peninsula, Turkey, Iran, India, Burma and Southeast Asia. There are two types of thalassemia including alpha and beta thalassemia.

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فراوانی نسبی اختلال عملکرد لوله ای کلیه در بیماران بتا تالاسمی مینور در شیراز

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APA: Copy

NAJAF POUR, MALIHEH, FARSHDOUSTI HAGH, MAJID, MOVASAGPOOR AKBARI, ALI AKBAR, HOSEIN POOR FEYZI, ABBAS ALI, & MALAKI, MAJID. (2015). GENETIC VARIATION IMPACTS IN PATIENTS WITH MAJOR BETA-THALASSEMIA (LETTER TO THE EDITOR). IRANIAN JOURNAL OF PUBLIC HEALTH, 44(5), 722-723. SID. https://sid.ir/paper/273901/en

Vancouver: Copy

NAJAF POUR MALIHEH, FARSHDOUSTI HAGH MAJID, MOVASAGPOOR AKBARI ALI AKBAR, HOSEIN POOR FEYZI ABBAS ALI, MALAKI MAJID. GENETIC VARIATION IMPACTS IN PATIENTS WITH MAJOR BETA-THALASSEMIA (LETTER TO THE EDITOR). IRANIAN JOURNAL OF PUBLIC HEALTH[Internet]. 2015;44(5):722-723. Available from: https://sid.ir/paper/273901/en

IEEE: Copy

MALIHEH NAJAF POUR, MAJID FARSHDOUSTI HAGH, ALI AKBAR MOVASAGPOOR AKBARI, ABBAS ALI HOSEIN POOR FEYZI, and MAJID MALAKI, “GENETIC VARIATION IMPACTS IN PATIENTS WITH MAJOR BETA-THALASSEMIA (LETTER TO THE EDITOR),” IRANIAN JOURNAL OF PUBLIC HEALTH, vol. 44, no. 5, pp. 722–723, 2015, [Online]. Available: https://sid.ir/paper/273901/en

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