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Hemoglobin
international journal for hemoglobin research
Volume 32, 2008 - Issue 6
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Original Article

α-Thalassemia Mutations in Khuzestan Province, Southwest Iran

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Pages 546-552 | Received 01 Jun 2008, Accepted 27 Jul 2008, Published online: 07 Jul 2009

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Read on this site (15)

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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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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Ya-Li Lei, Hong Sui, Yu-Juan Liu, Jun-Jun Pan, Yan-Hui Liu & Ji-Wu Lou. (2019) Molecular and Hematological Characterization of a Novel Translation Initiation Codon Mutation of the α2-Globin Gene (ATG>ATC or HBA2: c.3G>C). Hemoglobin 43:4-5, pages 241-244.
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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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John S. Waye, Barry Eng, Meredith Hanna, Betty-Ann Hohenadel, Lisa Nakamura & Lynda Walker. (2016) Novel Mutation of the Translation Initiation Codon of the α1-Globin Gene (ATG>AAG or HBA1:c.2T>A). Hemoglobin 40:5, pages 369-370.
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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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Reza Alibakhshi, Masomeh Mehrabi, Leila Omidniakan & Samaneh Shafieenia. (2015) The Spectrum of α-Thalassemia Mutations in Kermanshah Province, West Iran. Hemoglobin 39:6, pages 403-406.
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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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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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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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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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Azarkeivan Azita, Maryam Neishabury, Valeh Hadavi, Esteghamat Fatemehsadat, Saideh Enrahimkhani & Najmabadi Hossein. (2010) A REPORT OF 8 CASES WITH HEMOGLOBIN H DISEASE IN AN IRANIAN FAMILY. Pediatric Hematology and Oncology 27:5, pages 405-412.
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Valeh Hadavi, Maryam Jafroodi, Nima Hafezi-Nejad, Sousan Dehnadi Moghadam, Fatemeh Eskandari, Shahin Tarashohi, Hamideh Pourfahim, Christian Oberkanins, Hai-Yang Law & Hossein Najmabadi. (2009) α-Thalassemia Mutations in Gilan Province, North Iran. Hemoglobin 33:3-4, pages 235-241.
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Articles from other publishers (9)

Bijan Keikhaei, Mohammad Bahadoram, Mohammad-Reza Mahmoudian-Sani & Sara Bahadoram. (2021) Red cell distribution width as a differential parameter between iron deficiency anemia and a-thalassemia: an empirical approach. Pediatric Hematology/Oncology and Immunopathology 20:3, pages 156-157.
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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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Fatemeh Asadi, Seyedeh Moloud Rasouli Ghahfarokhi & Forough Talebi. (2019) Prevalence of Hemoglobin Mutations and Hemoglobinopathies in Masjed Soleiman County, Southeastern Iran. Medical Laboratory Journal 13:2, pages 48-54.
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Bijan Keikhaei, Pejman Slehi-fard, Gholamreza Shariati & Abbas Khosravi. (2018) Genetics of Iranian Alpha-Thalassemia Patients: A Comprehensive Original Study. Biochemical Genetics 56:5, pages 506-521.
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Masoomeh Sayahi, Farideh Ghanbari Mardasi & Masoomeh Salehi Kambo. (2017) Thalassemia Spectrum and Prenatal Diagnosis among Voluntary Couples in Shushtar City, during a Five Year Period. Gene, Cell and Tissue 4:4.
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Félix de la Fuente-Gonzalo, Jorge M. Nieto, Diego Velasco, Elena Cela, Germán Pérez, Ana Fernández-Teijeiro, Antonio Escudero, Ana Villegas, Fernando A. González-Fernández & Paloma Ropero. (2016) HB Puerta del Sol [HBA1:c.148A>C], HB Valdecilla [HBA2:c.3G>T], HB Gran Vía [HBA2:c.98T>G], HB Macarena [HBA2:c.358C>T] and HB El Retiro [HBA2:c.364_366dupGTG]: description of five new hemoglobinopathies. Clinical Chemistry and Laboratory Medicine (CCLM) 54:4.
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Sevcan Tug Bozdogan, Ozge Ozalp Yuregir, Nurhilal Buyukkurt, Huseyin Aslan, Zeynep Canan Ozdemir & Tomasz Gambin. (2014) Alpha-Thalassemia Mutations in Adana Province, Southern Turkey: Genotype-Phenotype Correlation. Indian Journal of Hematology and Blood Transfusion 31:2, pages 223-228.
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Muhammet Murat Celik, Ramazan Gunesacar, Gonul Oktay, Gulay Gulbol Duran & Hasan Kaya. (2013) Spectrum of α-thalassemia mutations including first observation of - -FIL deletion in Hatay Province, Turkey. Blood Cells, Molecules, and Diseases 51:1, pages 27-30.
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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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