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Hemoglobin
international journal for hemoglobin research
Volume 40, 2016 - Issue 1
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Original Article

Molecular Characterization of δ-Thalassemia in Iran

Alireza KordafshariDepartment of Molecular Medicine, Biotechnology Research Centre, Pasteur Institute of Iran, Tehran, Iran
,
Azam AmirianDepartment of Molecular Medicine, Biotechnology Research Centre, Pasteur Institute of Iran, Tehran, Iran
,
Sirous ZeinaliDepartment of Molecular Medicine, Biotechnology Research Centre, Pasteur Institute of Iran, Tehran, Iran
,
Atefeh ValaeiDepartment of Molecular Medicine, Biotechnology Research Centre, Pasteur Institute of Iran, Tehran, Iran
,
Fereshteh MaryamiDepartment of Molecular Medicine, Biotechnology Research Centre, Pasteur Institute of Iran, Tehran, Iran
&
Morteza KarimipoorDepartment of Molecular Medicine, Biotechnology Research Centre, Pasteur Institute of Iran, Tehran, IranCorrespondence[email protected]
Pages 44-47 | Received 27 May 2015, Accepted 31 Aug 2015, Published online: 12 Jan 2016

Citations (7)

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Read on this site (1)

Taner Karakaya, Fatma Silan & Ozturk Ozdemir. (2022) A New Mutation, Hb A2-Canakkale [δ10(A7)Ala→Val; HBD: c.32C>T], and Other Well-Known δ Variants Identified in a Selected Cohort with Low Hb A2 Levels. Hemoglobin 46:2, pages 87-90.
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Articles from other publishers (6)

Anping Xu, Mingyang Li, Yinghui Ye, Liping Li, Minjing Ma, Shang Ying Wu & Ling Ji. (2023) Mutational spectrum of HBD gene in the Chinese population: Description of 36 mutations including 11 novel variants . International Journal of Laboratory Hematology 45:6, pages 961-968.
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Chulikon Hanart, Kritsada Singha, Yotsombat Changtrakul, Supan Fucharoen & Hataichanok Srivorakun. (2023) Prospective screening for δ-hemoglobinopathies associated with decreased hemoglobin A2 levels or hemoglobin A2 variants: A single center experience. Clinica Chimica Acta 547, pages 117417.
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Keivan Moradi, Aboozar Mohammadi & Mohsen Kazeminia. (2021) In silico prediction of HBD gene variants in the Iranian population. Egyptian Journal of Medical Human Genetics 22:1.
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Kritsada Singha, Goonnapa Fucharoen & Supan Fucharoen. (2021) δ-Hemoglobinopathies in Thailand: screening, molecular basis, genotype-phenotype interaction, and implication for prevention and control of thalassemia. Annals of Hematology 100:8, pages 1953-1963.
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Meihuan Chen, Hailong Huang, Lingji Chen, Na Lin, Min Zhang, Yuan Lin & Liangpu Xu. (2020) First report of the spectrum of δ‐globin gene mutations among women of reproductive age in Fujian area—Discrimination of δ‐thalassemia, α‐thalassemia, and Iron Deficiency Anemia. Journal of Clinical Laboratory Analysis 34:11.
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H. Wajcman, M. Azimi, J. Cui, C. Hoppe, M. Flamini, C. Ho & S. Reddy. (2016) Hemoglobinopathy testing: the significance of accuracy and pitfalls in HbA 2 determination . International Journal of Laboratory Hematology 39:1.
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