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Hemoglobin
international journal for hemoglobin research
Volume 18, 1994 - Issue 3
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Original Article

The spectrum of β-thalassemia mutations in the oran region of algeria

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Pages 211-219 | Received 31 May 1993, Accepted 02 Feb 1994, Published online: 07 Jul 2009

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Read on this site (10)

Wissem Abdaoui, Djamel Eddine Benouareth, Amel Djenouni, Celine Renoux, Fatiha Grifi, Adel Gouri, Fateh Athamnia, Manel Benalioua & Philippe Joly. (2019) Genetic Background of β-Thalassemia in Northeast Algeria with Assessment of the Thalassemia Severity Score and Description of a new β0-Thalassemia Frameshift Mutation (HBB: c.374dup; p.Pro126Thrfs*15) . Hemoglobin 43:4-5, pages 223-228.
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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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Rami A. Jarjour, Hossam Murad, Faten Moasses & Walid Al-Achkar. (2014) Molecular Update of β-Thalassemia Mutations in the Syrian Population: Identification of Rare β-Thalassemia Mutations. Hemoglobin 38:4, pages 272-276.
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Essam H. Jiffri, Neda Bogari, Khaled H. Zidan, Salwa Teama & Nasser A. Elhawary. (2010) Molecular Updating of β-Thalassemia Mutations in the Upper Egyptian Population. Hemoglobin 34:6, pages 538-547.
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Roshan Colah, Ajit Gorakshakar & Anita Nadkarni. (2010) Global burden, distribution and prevention of β-thalassemias and hemoglobin E disorders. Expert Review of Hematology 3:1, pages 103-117.
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Nassima Boudrahem-Addour, Nadia Zidani, Nathalie Carion, Dominique Labie, Meriem Belhani & Cherif Beldjord. (2009) Molecular Heterogeneity of β-Thalassemia in Algeria: How to Face Up to a Major Health Problem. Hemoglobin 33:1, pages 24-36.
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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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Slaheddine Fattoum, Taeib Messaoud & Amina Bibi. (2004) Molecular Basis of β‐Thalassemia in the Population of Tunisia. Hemoglobin 28:3, pages 177-187.
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K. Kyriacou, F. Al Quobaili, E. Pavlou, G. Christopoulos, P. Ioannou & M. Kleanthous. (2000) Molecular Characterization of β-Thalassemia in Syria. Hemoglobin 24:1, pages 1-13.
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P. Lacan, A. Francina, D. Prome, J. Delaunay, F. Galacteros & H. Wajcman. (1996) Hb Aubenas [β26(B8)GLU→GLY]: A new Variant Normally Synthesized, Affecting the Same Codon as in Hb E. Hemoglobin 20:2, pages 113-124.
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Articles from other publishers (9)

Ekta Rao, Sandip Kumar Chandraker, Mable Misha Singh & Ravindra Kumar. (2024) Global distribution of β-thalassemia mutations: An update. Gene 896, pages 148022.
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Carinna Hockham, Frédéric B. Piel, Sunetra Gupta & Bridget S. Penman. (2015) Understanding the contrasting spatial haplotype patterns of malaria-protective β-globin polymorphisms. Infection, Genetics and Evolution 36, pages 174-183.
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Shirley Henderson, Adele Timbs, Janice McCarthy, Alice Gallienne, Margaretha Van Mourik, Gillian Masters, Alison May, Mohamed S.M. Khalil, Anna Schuh & John Old. (2009) Incidence of haemoglobinopathies in various populations — The impact of immigration. Clinical Biochemistry 42:18, pages 1745-1756.
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Imane AgoutiCatherine BadensAhmed AbouyoubNicolas LevyMohcine Bennani. (2008) Molecular Basis of β-Thalassemia in Morocco: Possible Origins of the Molecular Heterogeneity. Genetic Testing 12:4, pages 563-568.
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Amel Haj Khelil, Sandrine Laradi, Abdelhedi Miled, Ghazi Omar Tadmouri, Jemni Ben Chibani & Pascale Perrin. (2004) Clinical and molecular aspects of haemoglobinopathies in Tunisia. Clinica Chimica Acta 340:1-2, pages 127-137.
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Noriko Fujihara, Minoru Tozuka, Ichiro Ueno, Kazuyoshi Yamauchi, Ritsuko Nakagoshi, Shinsuke Ishikawa, Masako Hirota, Nobuo Okumura, Eizaburo Ishii & Tsutomu Katsuyama. (2002) Novel β‐thalassemia trait (IVS I‐1 G→C) in a Japanese family. American Journal of Hematology 72:1, pages 64-66.
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G.O. Tadmouri, O. Bileno?lu, S. Kantarc?H. Kayserili, P. Perrin & A.N. Ba?ak. (2000) A rare mutation [IVS-I-130 (G-A)] in a Turkish ?-thalassemia major patient. American Journal of Hematology 63:4, pages 223-225.
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Pascale Perrin, Rachid Bouhassa, Leı̈la Mselli, Nathalie Garguier, Victor-Marc Nigon, Chouki Bennani, Dominique Labie & Guy Trabuchet. (1998) Diversity of sequence haplotypes associated with β-thalassaemia mutations in Algeria: implications for their origin. Gene 213:1-2, pages 169-177.
Crossref
Philippe Lacan, Jean Kister, Alain Francina, Gérard Souillet, Frédéric Galactéros, Jean Delaunay & Henri Wajcman. (1996) Hemoglobin debrousse (β96[FG3]Leu → Pro): A new unstable hemoglobin with twofold increased oxygen affinity. American Journal of Hematology 51:4, pages 276-281.
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