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Hemoglobin
international journal for hemoglobin research
Volume 33, 2009 - Issue 3-4
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Original Article

α-Thalassemia Mutations in Gilan Province, North Iran

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Pages 235-241 | Received 03 Feb 2009, Accepted 02 Mar 2009, Published online: 15 Sep 2009

Keep up to date with the latest research on this topic with citation updates for this article.

Read on this site (21)

Hossam Murad, Faten Moassas, Bouthina Ali, Eiad Katranji & Yasser Mukhalalaty. (2023) The Spectrum of α-Thalassemia Mutations in Syrian Patients. Hemoglobin 47:6, pages 245-248.
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Keivan Moradi, Mozaffar Aznab, Azam Azimi, Mostafa Biglari, Samaneh Shafieenia & Reza Alibakhshi. (2022) α-Thalassemia Mutations in Ilam Province, West Iran. Hemoglobin 46:3, pages 147-152.
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Mina Ebrahimi, Javad Mohammadi-Asl & Fakher Rahim. (2021) The worldwide molecular spectrum and distribution of thalassaemia: a systematic review. Annals of Human Biology 48:4, pages 307-312.
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Sara Alimohammadi-Bidhendi, Sarah Azadmehr, Masoumeh Razipour, Sirous Zeinali, Maryam Eslami & Elham Davoudi-Dehaghani. (2021) Regulatory Mutation Study in Cases with Unsolved Hypochromic Microcytic Anemia and α-Major Regulatory Element Haplotype Analysis in Iran. Hemoglobin 45:1, pages 37-40.
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Keivan Moradi, Mozaffar Aznab, Mostafa Biglari, Samaneh Shafieenia, Azam Azimi, Nushin Bijari & Reza Alibakhshi. (2020) Molecular Genetic Analysis of α-Thalassemia in Hamadan Province, West Iran. Hemoglobin 44:5, pages 319-324.
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Arwa Z. Al-Riyami, Shahina Daar, Salam Al Kindi, Ali Al Madhani, Yasser Wali, Mohammed Al Rawahi & Shoaib Al Zadjali. (2020) α-Globin Genotypes Associated with Hb H Disease: A Report from Oman and a Review of the Literature from the Eastern Mediterranean Region. Hemoglobin 44:1, pages 20-26.
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Qiang Zhang, Xin Fan, Mingli Xu, Yijia Zhang, Huiling Xu, Xiaojun Wen & Wanjun Zhou. (2017) Hb H Disease Caused by Multiple Mutations in the Polyadenylation Signal Site and − −SEA/αα. Hemoglobin 41:3, pages 189-192.
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Hajar Eftekhari, Ahmad Tamaddoni, Hassan Mahmoudi Nesheli, Mohsen Vakili, Sadegh Sedaghat, Ali Banihashemi, Mandana Azizi, Reza Youssefi Kamangar & Haleh Akhavan-Niaki. (2017) A Comprehensive Molecular Investigation of α-Thalassemia in an Iranian Cohort from Different Provinces of North Iran. Hemoglobin 41:1, pages 32-37.
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Sima M. Derakhshan, Mahmoud S. Khaniani, Fateme Afkhami & Abbasali H. PourFeizi. (2016) Molecular Study of Deletional and Nondeletional Mutations on the α-Globin Locus in the Azeri Population of Northwestern Iran. Hemoglobin 40:5, pages 319-322.
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Abbas Khosravi, Mohammadali Jalali-Far, Najmaldin Saki, Hossein Hosseini, Hamid Galehdari, Omid Kiani-Ghalesardi, Mostafa Paridar, Azita Azarkeivan & Kabir Magaji-Hamid. (2016) Evaluation of α-Globin Gene Mutations Among Different Ethnic Groups in Khuzestan Province, Southwest Iran. Hemoglobin 40:2, pages 113-117.
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Samaneh Farashi, Nooshin Bayat, Shadi Vakili, Negin Faramarzi Garous, Mehri Ashki, Hashem Imanian, Hossein Najmabadi & Azita Azarkeivan. (2016) Point mutations which should not be overlooked in Hb H disease. Expert Review of Hematology 9:1, pages 107-113.
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Javad Dehbozorgian, Mohamad Moghadam, Saeed Daryanoush, Sezaneh Haghpanah, Jaber Imani fard, Azam Aramesh, Amin Shahsavani & Mehran Karimi. (2015) Distribution of alpha-thalassemia mutations in Iranian population. Hematology 20:6, pages 359-362.
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Samaneh Farashi, Negin Faramarzi Garous, Fatemeh Zeinali, Shadi Vakili, Mehri Ashki, Hashem Imanian, Hossein Najmabadi, Azita Azarkeivan & Ahmad Tamaddoni. (2015) A 21 Nucleotide Duplication on the α1- and α2-Globin Genes Involves a Variety of Hypochromic Microcytic Anemias, From Mild to Hb H Disease. Hemoglobin 39:3, pages 196-200.
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Nima Hafezi-Nejad, Mohsen Khosravi, Nooshin Bayat, Ariana Kariminejad, Valeh Hadavi, Christian Oberkanins, Azita Azarkeivan & Hossein Najmabadi. (2014) Characterizing a Cohort of α-Thalassemia Couples Collected During Screening for Hemoglobinopathies: 14 Years of an Iranian Experience. Hemoglobin 38:3, pages 153-157.
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Arezo Karamzade, Hadi Mirzapour, Majid Hoseinzade, Sara Asadi, Tahere Gholamrezapour, Parvaneh Tavakoli & Mansoor Selebi. (2014) α-Globin Gene Mutations in Isfahan Province, Iran. Hemoglobin 38:3, pages 161-164.
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Nooshin Bayat, Samaneh Farashi, Nima Hafezi-Nejad, Negin Faramarzi, Mehri Ashki, Shadi Vakili, Hashem Imanian, Mohsen Khosravi, Azita Azar-Keivan & Hossein Najmabadi. (2013) Novel Mutations Responsible for α-Thalassemia in Iranian Families. Hemoglobin 37:2, pages 148-159.
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Nasir A.S. Al-Allawi, Sana D. Jalal, Najeeb S. Rasheed, Nooshin Bayat, Hashem Imanian, Hossein Najmabadi & Azad Faraj. (2013) The Spectrum of α-Thalassemia Mutations in the Kurdish Population of Northeastern Iraq. Hemoglobin 37:1, pages 56-64.
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Faramarzi Hossein, Rastegar Mohsen, Moghadami Mohsen & Mohammad Taheri. (2012) α-Thalassemia Mutations in Two Provinces of Southern Iran: FARS & Kohkeloye and Bouyer Ahmad. Hemoglobin 36:2, pages 139-143.
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Haleh Akhavan-Niaki, Ali Banihashemi, Amrollah Mostafazadeh, Vahid Kholghi Oskooei, Mandana Azizi, Reza Youssefi Kamangar & Maryam Mitra Elmi. (2012) Simultaneous Detection of Hb Constant Spring (α142, TAA>CAA, α2) and The α2 IVS-I Donor Site (−TGAGG) Deletion by a Simple Polymerase Chain Reaction-Based Method in Iran. Hemoglobin 36:2, pages 124-130.
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Saedieh Ebrahimkhani, Azita Azarkeivan, Nooshin Bayat, Mahdieh Houry-Parvin, Sayeh Jalil-Nejad, Shima Zand, Zahra Golkar, Valeh Hadavi, Hashem Imanian, Christian Oberkanins & Hossein Najmabadi. (2011) Genotype-Phenotype Correlation In Iranian Patients With Hb H Disease. Hemoglobin 35:1, pages 40-46.
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Nasrollah Saleh-Gohari & Arezo Khosravi-Mashizi. (2010) Spectrum of α-Globin Gene Mutations in the Kerman Province of Iran. Hemoglobin 34:5, pages 451-460.
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Articles from other publishers (5)

Mona Asghari Ahmadabad, Noushin Pourreza, Setareh Ramezanpour, Adel Baghersalimi, Mersedeh Enshaei, Marjan Askari, Amirhossein Alizadeh, Elahe Izadi & Bahram Darbandi. (2023) An analysis of the distribution and spectrum of alpha thalassemia mutations in Rasht City, North of Iran. Frontiers in Pediatrics 11.
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Seyed Mohammad Bagher Hashemi‐Soteh, Hossein Karami, Seyed Saeid Mousavi, Touraj Farazmandfar & Ahmad Tamadoni. (2019) Alpha‐globin gene mutation spectrum in patients with microcytic hypochromic anemia from Mazandaran Province, Iran. Journal of Clinical Laboratory Analysis 34:1.
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Paloma Ropero, Ana Villegas, Jorge M. Nieto, Fernando A. González & Rafael Martínez. (2019) Novel nonsense mutation in the α1-globin gene [HBA1:C.49A>T] is responsible for non-deletion α-thalassemia. Clinical Biochemistry 63, pages 139-142.
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Zohreh Rahimi. (2013) Genetic Epidemiology, Hematological and Clinical Features of Hemoglobinopathies in Iran. BioMed Research International 2013, pages 1-10.
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Maryam Neishabury, Azita Azarkeivan, Christian Oberkanins, Seyedeh Sedigheh Abedini, Shahbaz Zamani & Hossein Najmabadi. (2011) Analyzing 5′HS3 and 5′HS4 LCR core regions and NF-E2 in Iranian thalassemia intermedia patients with normal or carrier status for beta-globin mutations. Blood Cells, Molecules, and Diseases 46:3, pages 201-205.
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