Letter to the Editor, The Prevalence of Hemoglobinopathies in Reference Laboratory of Kermanshah, Western Iran

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EBRAHIMI ZOHREH; NAJAFI Sozan; MOGHOFEHIE Lila; AMIRI EBRAHIM; VAISI RAYGANI ASAD; RAHIMI ZIBA

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Journal: Iranian Journal of Public Health Year:2019 | Volume:48 | Issue:2 Page(s): 359-361

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Title

Letter to the Editor, The Prevalence of Hemoglobinopathies in Reference Laboratory of Kermanshah, Western Iran

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Abstract

Dear Editor-in-Chief Hemoglobinopathies are a group of autosomal recessive disorders that consisted of structural variants of hemoglobins (S, C, D, O, Q, Setif) and thalassemia syndromes (𝛼-and 𝛽-thalassemia) (1). The hemoglobin S (Hb S) is the most clinically important structural variant of hemoglobin that results from substitution of va-line for glutamic acid at position 6 of the 𝛽-chain (2). The Hb D-Punjab (D-Los Angeles) results from substitution of glutamine for glutamic acid at position of 121 of the 𝛽-globin chain (3). . . .

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APA: Copy

EBRAHIMI, ZOHREH, NAJAFI, Sozan, MOGHOFEHIE, Lila, AMIRI, EBRAHIM, VAISI RAYGANI, ASAD, & RAHIMI, ZIBA. (2019). Letter to the Editor, The Prevalence of Hemoglobinopathies in Reference Laboratory of Kermanshah, Western Iran. IRANIAN JOURNAL OF PUBLIC HEALTH, 48(2), 359-361. SID. https://sid.ir/paper/274995/en

Vancouver: Copy

EBRAHIMI ZOHREH, NAJAFI Sozan, MOGHOFEHIE Lila, AMIRI EBRAHIM, VAISI RAYGANI ASAD, RAHIMI ZIBA. Letter to the Editor, The Prevalence of Hemoglobinopathies in Reference Laboratory of Kermanshah, Western Iran. IRANIAN JOURNAL OF PUBLIC HEALTH[Internet]. 2019;48(2):359-361. Available from: https://sid.ir/paper/274995/en

IEEE: Copy

ZOHREH EBRAHIMI, Sozan NAJAFI, Lila MOGHOFEHIE, EBRAHIM AMIRI, ASAD VAISI RAYGANI, and ZIBA RAHIMI, “Letter to the Editor, The Prevalence of Hemoglobinopathies in Reference Laboratory of Kermanshah, Western Iran,” IRANIAN JOURNAL OF PUBLIC HEALTH, vol. 48, no. 2, pp. 359–361, 2019, [Online]. Available: https://sid.ir/paper/274995/en

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