Publication Cover
Hemoglobin
international journal for hemoglobin research
Volume 46, 2022 - Issue 3
93
Views
4
CrossRef citations to date
0
Altmetric
Original Articles

α-Thalassemia Mutations in Ilam Province, West Iran

, , , , &
Pages 147-152 | Received 10 Oct 2019, Accepted 02 Nov 2019, Published online: 19 Feb 2020

References

  • Onay H, Aykut A, Karaca E, et al. Molecular spectrum of α-globin gene mutations in the Aegean region of Turkey: first observation of three α-globin gene mutations in the Turkish population. Int J Hematol. 2015;102(1):1–6.
  • Moradi K, Aznab M, Tahmasebi S, et al. The spectrum of α-thalassemia mutations in the Lak population of Iran. Hemoglobin. 2019;43(2):107–111.
  • Phylipsen M, Prior JF, Lim E, et al. Thalassemia in Western Australia: 11 novel deletions characterized by multiplex ligation-dependent probe amplification. Blood Cell Mol Dis. 2010;44(3):146–151.
  • Mahdavi MR, Hojjati MT, Roshan P. A review on thalassemia and related complications. J Manzandaran Univ Med Sci. 2013;23(103):139–149.
  • Samavat A, Modell B. Iranian national thalassaemia screening programme. Br Med J. 2004;329(7475):1134–1137.
  • Aliakbari M, Gheitasi M, Anonby E. On language distribution in Ilam Province, Iran Stud. 2015;48(6):835–850.
  • Alibakhshi R, Mehrabi M, Omidniakan L, et al. The spectrum of β-thalassemia mutations in Kermanshah Province. West Iran. Hemoglobin. 2015;39(6):403–406.
  • Alibakhshi R, Khalegi S, Akramipour R, et al. Molecular analysis of α globin genes non deletional mutations in α thalassemia patients in Kermanshah Province. Razi J Med Sci. 2014;21(118):13–21.
  • Saleh-Gohari N, Khosravi-Mashizi A. Spectrum of α-globin gene mutations in the Kerman Province of Iran. Hemoglobin. 2010;34(5):451–460.
  • Miri-Moghaddam E, Nikravesh A, Gasemzadeh N, et al. Spectrum of α-globin gene mutations among premarital Baluch couples in southeastern Iran. Int J Hematol Oncol Stem Cell Res. 2015;9(3):138–142.
  • Hossein F, Mohsen R, Mohsen M, et al. α-Thalassemia mutations in two provinces of Southern Iran: Fars & Kohkeloye and Bouyer Ahmad. Hemoglobin. 2012;36(2):139–143.
  • Dehbozorgian J, Moghadam M, Daryanoush S, et al. Distribution of α-thalassemia mutations in Iranian population. Hematology. 2015;20(6):359–362.
  • Hashemi-Soteh SMB, Karami H, Mousavi SS, et al. α Globin gene mutation spectrum in patients with microcytic hypochromic anemia from Mazandaran Province, Iran. J Clin Lab Anal. 2020;34(1):e23018.
  • Eftekhari H, Tamaddoni A, Mahmoudi Nesheli H, et al. A comprehensive molecular investigation of α-thalassemia in an Iranian cohort from different provinces of North Iran. Hemoglobin. 2017;41(1):32–37.
  • Zarbakhsh B, Farshadi E, Ariani Kashani A, et al. Molecular study of α-thalassemia mutations in Iranian potential carriers. Sci J Iran Blood Transfus Organ. 2010;7(2):70–77.
  • Hadavi V, Taromchi AH, Malekpour M, et al. Elucidating the spectrum of α-thalassemia mutations in Iran. Haematologica. 2007;92(7):992–993.
  • Keikhaei B, Slehi-Fard P, Shariati G, et al. Genetics of Iranian α-thalassemia patients: a comprehensive original study. Biochem Genet. 2018;56(5):506–521.
  • Derakhshan SM, Khaniani MS, Afkhami F, et al. Molecular study of deletional and nondeletional mutations on the α-globin locus in the Azeri population of Northwestern Iran. Hemoglobin. 2016;40(5):319–322.
  • Valaei A, Karimipoor M, Kordafshari A, et al. Molecular basis of α-Thalassemia in Iran. Iran Biomed J. 2018;22(1):6–14.
  • Harteveld CL, Higgs DR. α-Thalassaemia. Orphanet J Rare Dis. 2010;5(1):13.
  • Tamaddoni A, Hadavi V, Nejad NH, et al. α-Thalassemia mutation analyses in Mazandaran Province. North Iran. Hemoglobin. 2009;33(2):115–123.
  • Hadavi V, Jafroodi M, Hafezi-Nejad N, et al. α-Thalassemia mutations in Gilan Province. North Iran. Hemoglobin. 2009;33(3–4):235–241.
  • Al-Allawi NA, Jalal SD, Rasheed NS, et al. The spectrum of α-thalassemia mutations in the Kurdish population of Northeastern Iraq. Hemoglobin. 2013;37(1):56–64.
  • Orkin SH, Goff SC, Hechtman RL. Mutation in an intervening sequence splice junction in man. Proc Natl Acad Sci USA. 1981;78(8):5041–5045.
  • Galanello R, Sollaino C, Paglietti E, et al. α-Thalassemia carrier identification by DNA analysis in the screening for thalassemia. Am J Hematol. 1998;59(4):273–278.
  • Usman K, Syed ZA, Rao AA. Reference range values of haematological parameters in healthy Pakistani adults. Pak J Physiol. 2007;3(1):19–22.
  • Grau M, Cremer JM, Bloch W. Comparisons of blood parameters, red blood cell deformability and circulating nitric oxide between males and females considering hormonal contraception: a longitudinal gender study. Front Psychol. 2018;9:1835. eCollection 2018.
  • Denic S, Agarwal MM, Al Dabbagh B, et al. Hemoglobin A2 lowered by iron deficiency and α-thalassemia: should screening recommendation for β-thalassemia change? ISRN Hematol. 2013;2013:1.
  • Bozdogan ST, Yuregir OO, Buyukkurt N, et al. α-Thalassemia mutations in Adana Province, southern Turkey: genotype-phenotype correlation. Indian J Hematol Blood Transfus. 2015;31(2):223–228.
  • Al-Allawi NA, Badi AI, Imanian H, et al. Molecular characterization of β-thalassemia in the Dohuk region of Iraq. Hemoglobin. 2009;33(1):37–44.

Reprints and Corporate Permissions

Please note: Selecting permissions does not provide access to the full text of the article, please see our help page How do I view content?

To request a reprint or corporate permissions for this article, please click on the relevant link below:

Academic Permissions

Please note: Selecting permissions does not provide access to the full text of the article, please see our help page How do I view content?

Obtain permissions instantly via Rightslink by clicking on the button below:

If you are unable to obtain permissions via Rightslink, please complete and submit this Permissions form. For more information, please visit our Permissions help page.