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Rawand Shamoon, Ahmed Yassin & Amir Charkaneh. (2023) Detection of a Rare Mutation in the Initiation Codon of the β-Globin Gene (HBB:C.2T > C; P.Met1Thr). Hemoglobin 47:3, pages 118-121.
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Ajit C. Gorakshakar, Pearl V. Breganza, Stacy P. Colaco, Roshan F. Shaikh, Meenu Y. Bohra, Pratibha M. Sawant, Anita H. Nadkarni, Roshan B. Colah & Kanjaksha K. Ghosh. (2018) Rare β- and δ-Globin Gene Mutations in the Pathare Prabhus: Original Inhabitants of Mumbai, India. Hemoglobin 42:5-6, pages 297-301.
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Rakesh Kumar, Chandan Sagar, Dharmesh Sharma & Purnima Kishor. (2015) β-Globin Genes: Mutation Hot-Spots in the Global Thalassemia Belt. Hemoglobin 39:1, pages 1-8.
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Amina Bibi, Taieb Messaoud, Cherif Beldjord & Slaheddine Fattoum. (2006) Detection of Two Rare β-Thalassemia Alleles Found in the Tunisian Population: Codon 47 (+A) and Codons 106/107 (+G). Hemoglobin 30:4, pages 437-447.
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Amina Bibi, Taieb Messaoud & Slaheddine Fattoum. (2006) Haplotypes Linked to Three Rare β-Thalassemia Mutations, Originally Reported in Tunisia. Hemoglobin 30:2, pages 175-181.
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Shaheen N. Khan, Farrukh Hasan, Carla Sollaino, Luciana Perseu & Sheikh Riazuddin. (2003) Molecular Characterization of α‐Thalassemia in Pakistan. Hemoglobin 27:3, pages 161-166.
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John M. Old, Shaheen N. Khan, Ishwar Verma, Suthat Fucharoen, Marina Kleanthous, Panos Ioannou, Navaratnam Kotea, Christopher Fisher, Sheikh Riazuddin, Renu Saxena, Pranee Winichagoon, Kyriacos Kyriacou, Faizeh Al-Quobaili & Baldip Khan. (2001) A MULTI-CENTER STUDY IN ORDER TO FURTHER DEFINE THE MOLECULAR BASIS OF β-THALASSEMIA IN THAILAND, PAKISTAN, SRI LANKA, MAURITIUS, SYRIA, AND INDIA, AND TO DEVELOP A SIMPLE MOLECULAR DIAGNOSTIC STRATEGY BY AMPLIFICATION REFRACTORY MUTATION SYSTEM-POLYMERASE CHAIN REACTION. Hemoglobin 25:4, pages 397-407.
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Articles from other publishers (7)
Alexander W. Macharia, George Mochamah, Johnstone Makale, Thad Howard, Neema Mturi, Peter Olupot-Olupot, Anna Färnert, Russell E. Ware & Thomas N. Williams. (2022) Case Report: β-thalassemia major on the East African coast. Wellcome Open Research 7, pages 188.
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L. Jouini, C. A. Sahli, N. Laaouini, F. Ouali, I. Ben Youssef, B. Dakhlaoui, R. Othmeni, F. Ouennich, S. Hadj Fredj, H. Siala, M. Becher, N. E. Toumi, S. Fattoum, R. Hafsia, A. Bibi & T. Messaoud. (2013) Association between clinical expression and molecular heterogeneity in β-thalassemia Tunisian patients. Molecular Biology Reports 40:11, pages 6205-6212.
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Latifa Jouini, Amina Bibi, Faida Ouali, Sondess Hadj Fredj, Fekria Ouennich, Hajer Siala, Taieb Messaoud & Slaheddine Fattoum. (2011) Contribution of β-globin cluster polymorphisms to raise fetal hemoglobin levels in normal adults. Molecular Biology Reports 39:4, pages 4619-4625.
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V. VIPRAKASIT, W. CHINCHANG, L. SUWANTHOL & V. S. TANPHAICHITR. (2005) Common origin of a rare beta-globin initiation codon mutation (ATGAGG) in Asians. Clinical and Laboratory Haematology 27:6, pages 409-415.
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Anju Gupta, Yukio Hattori, Usha R. Gupta, Swati Sarwai, Nitu Nigam, Pragya Singhal & Sarita Agarwal. (2003) Molecular Genetic Testing of β-Thalassemia Patients of Indian Origin and a Novel 8-bp Deletion Mutation at Codons 36/37/38/39. Genetic Testing 7:2, pages 163-168.
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Anju Gupta, Yukio Hattori & Sarita Agarwal. (2002) Initiation codon mutation in an Asian Indian family. American Journal of Hematology 71:2, pages 134-136.
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