مرکز اطلاعات علمی Scientific Information Database (SID) - Trusted Source for Research and Academic Resources

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Cites:

3

Information Journal Paper

Title

DETECTION OF RARE AND UNKNOWN MUTATIONS IN β- TALASSEMIA TRAITS IN IRAN

Pages

  11-14

Abstract

BETA-THALASSEMIA, by its high frequency and heterogeneity, constitutes a real problem of health in IRAN. About 13 beta globin mutations encompass 70-90% of mutations spectrum in IRAN, the rest are rare or unknown. In this study six mutations of the codon IVSI-130(G-C), Frl6 (-C), codon35 (-C), fr23/24(-G), codon8 (+G) and codon 20 (GTG-GAG) were recognized and added to spectrum of beta globin mutations in IRAN, using ARMS/PCR and DNA sequencing. Three latter cases are reported for first time.

Cites

References

Cite

APA: Copy

HABIBI ROUDKENAR, M., DERAKHSHANDEH PEYKAR, P., FARHOUD, D.D., & NAJMABADI, H.. (2003). DETECTION OF RARE AND UNKNOWN MUTATIONS IN β- TALASSEMIA TRAITS IN IRAN. IRANIAN JOURNAL OF PUBLIC HEALTH, 32(1), 11-14. SID. https://sid.ir/paper/272003/en

Vancouver: Copy

HABIBI ROUDKENAR M., DERAKHSHANDEH PEYKAR P., FARHOUD D.D., NAJMABADI H.. DETECTION OF RARE AND UNKNOWN MUTATIONS IN β- TALASSEMIA TRAITS IN IRAN. IRANIAN JOURNAL OF PUBLIC HEALTH[Internet]. 2003;32(1):11-14. Available from: https://sid.ir/paper/272003/en

IEEE: Copy

M. HABIBI ROUDKENAR, P. DERAKHSHANDEH PEYKAR, D.D. FARHOUD, and H. NAJMABADI, “DETECTION OF RARE AND UNKNOWN MUTATIONS IN β- TALASSEMIA TRAITS IN IRAN,” IRANIAN JOURNAL OF PUBLIC HEALTH, vol. 32, no. 1, pp. 11–14, 2003, [Online]. Available: https://sid.ir/paper/272003/en

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