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Information Journal Paper

Title

MOLECULAR STUDIES ON BETA-THALASSEMIA MUTATIONS IN BUSHEHR PROVINCE

Pages

  83-89

Abstract

BETA-THALASSEMIA is a major hereditary blood disorder in Iran. This disease is more prevalent in provinces of the south and north of Iran. In this MUTATIONal screening study using ARMS/PCR technique was conducted on 104 blood samples of thalassemic patients from Bushehr Province who receiving regular blood transfusions. We used 12 ARMS primers. MUTATIONs in 81.73% of chromosomes were detected. The frequency of detected MUTATIONs were the following: IvI 3' end (24.04%), IvsII-1 (12.98%), IvsI-1 (9.13%), Fr 8,9 (8.17%), IvsI-5 (7.69%), IvsI-110 (5. 77%), codon 30 (3.36%), codun 39 (3.36%), IvsII-745 (3.36%), codon 5 (2.40%), IvsaI-6(1.44%); and no codon 44 MUTATION was detected. Therefore, the most common MUTATION among thalassemic patient in Bushehr Province was - 25bp deletion in IvsI.  

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  • Cite

    APA: Copy

    KHODAEI, H., ZEINALI, C., & DELMAGHANI, S.. (2001). MOLECULAR STUDIES ON BETA-THALASSEMIA MUTATIONS IN BUSHEHR PROVINCE. IRANIAN SOUTH MEDICAL JOURNAL (ISMJ), 3(2), 83-89. SID. https://sid.ir/paper/34051/en

    Vancouver: Copy

    KHODAEI H., ZEINALI C., DELMAGHANI S.. MOLECULAR STUDIES ON BETA-THALASSEMIA MUTATIONS IN BUSHEHR PROVINCE. IRANIAN SOUTH MEDICAL JOURNAL (ISMJ)[Internet]. 2001;3(2):83-89. Available from: https://sid.ir/paper/34051/en

    IEEE: Copy

    H. KHODAEI, C. ZEINALI, and S. DELMAGHANI, “MOLECULAR STUDIES ON BETA-THALASSEMIA MUTATIONS IN BUSHEHR PROVINCE,” IRANIAN SOUTH MEDICAL JOURNAL (ISMJ), vol. 3, no. 2, pp. 83–89, 2001, [Online]. Available: https://sid.ir/paper/34051/en

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