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Hemoglobin
international journal for hemoglobin research
Volume 28, 2004 - Issue 1
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Original Article

The β‐Thalassemia Mutation/Haplotype Distribution in the Moroccan Population

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Pages 25-37 | Received 08 Aug 2003, Accepted 15 Oct 2003, Published online: 24 Aug 2009

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Luis J. Sánchez-Martínez, Candela L. Hernández, Juan N. Rodríguez, Jean M. Dugoujon, Andrea Novelletto, Paloma Ropero, Luisa Pereira & Rosario Calderón. (2021) Genetic variation patterns of β-thalassemia in Western Andalusia (Spain) reveal a structure of specific mutations within the Iberian Peninsula. Annals of Human Biology 48:5, pages 406-417.
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Aisha Moeen Khan, Asma Mohammed Al-Sulaiti, Salma Younes, Mohamed Yassin & Hatem Zayed. (2021) The spectrum of beta-thalassemia mutations in the 22 Arab countries: a systematic review. Expert Review of Hematology 14:1, pages 109-122.
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Hossam Murad, Faten Moassas, Ifad Ghoury & Yasser Mukhalalaty. (2018) Haplotype Analysis of Three Common β-Thalassemia Mutations in Syrian Patients. Hemoglobin 42:5-6, pages 302-305.
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Hossam Murad, Faten Moasses, Amir Dabboul, Yasser Mukhalalaty, Ahmad Omar Bakoor, Walid Al-Achkar & Rami A. Jarjour. (2018) Geographical distribution of β-globin gene mutations in Syria. Hematology 23:9, pages 697-704.
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Faten Moassas, Ayman Alabloog & Hossam Murad. (2018) Description of a Rare β-Globin Gene Mutation: –86 (C>G) (HBB: c.-136C>G) Observed in a Syrian Family. Hemoglobin 42:3, pages 203-205.
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Laudy Cherry, Carla Calo, Rodica Talmaci, Pascale Perrin & Lucian Gavrila. (2016) β-Thalassemia Haplotypes in Romania in the Context of Genetic Mixing in the Mediterranean Area. Hemoglobin 40:2, pages 85-96.
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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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Amel Haj Khelil, Sabri Denden, Nadia Leban, Houria Daimi, Ramzi Lakhdhar, Gérard Lefranc, Jemni Ben Chibani & Pascale Perrin. (2010) Hemoglobinopathies in North Africa: A Review. Hemoglobin 34:1, pages 1-23.
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Imane Agouti, Mohcine Bennani, Nicolas Levy, Piero Giordano & Catherine Badens. (2009) The Rare Codon 24 (T>A) (β+) Mutation in Association with the Common Codon 39 (C> T) (β0) Mutation Causes Transfusion-Dependent β-Thalassemia in a Moroccan Patient. Hemoglobin 33:2, pages 150-154.
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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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Imane Agouti, Catherine Badens, Ahmed Abouyoub, Mohamed Khattab, Fouad Sayah, Amina Barakat & Mohcine Bennani. (2007) Genotypic Correlation Between Six Common β-Thalassemia Mutations and the XmnI Polymorphism in the Moroccan Population. Hemoglobin 31:2, pages 141-149.
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Articles from other publishers (11)

Ihab Belmokhtar, Saida Lhousni, Mounia Elidrissi Errahhali, Ayad Ghanam, Manal Elidrissi Errahhali, Zaina Sidqi, Meryem Ouarzane, Majida Charif, Mohammed Bellaoui, Redouane Boulouiz & Noufissa Benajiba. (2022) Molecular heterogeneity of β‐thalassemia variants in the Eastern region of Morocco. Molecular Genetics & Genomic Medicine 10:8.
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Zhihua Jiang, Hong-yuan Luo, Shengwen Huang, John J. Farrell, Lance Davis, Roger Th?berge, Katherine A. Benson, Suchada Riolueang, Vip Viprakasit, Nasir A.S. Al-Allawi, Sule ?nal, Fatma G?mr?k, Nejat Akar, A. Nazli Ba?ak, Leonor Osorio, Catherine Badens, Serge Pissard, Philippe Joly, Andrew D. Campbell, Patrick G. Gallagher, Martin H. Steinberg, Bernard G. Forget & David H.K. Chui. (2016) The genetic basis of asymptomatic codon 8 frame-shift ( HBB :c25_26delAA) ? 0 -thalassaemia homozygotes . British Journal of Haematology 172:6, pages 958-965.
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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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Leonor Osório Almeida. (2015) Human Gene Mutations and Migratory Flows—Portugal and the Mediterranean. Advances in Anthropology 05:03, pages 164-169.
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Hanan A. Hamamy & Nasir A. S. Al-Allawi. (2012) Epidemiological profile of common haemoglobinopathies in Arab countries. Journal of Community Genetics 4:2, pages 147-167.
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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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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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Zohreh Rahimi, Adriana Muniz, Reza Akramipour, Fareidon Tofieghzadeh, Hadi Mozafari, Asad Vaisi-Raygani & Abbas Parsian. (2009) Haplotype analysis of beta thalassemia patients in Western Iran. Blood Cells, Molecules, and Diseases 42:2, pages 140-143.
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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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P. Eaton, G. Doria, E. Pereira, P.V. Baptista & R. Franco. (2007) Imaging Gold Nanoparticles for DNA Sequence Recognition in Biomedical Applications. IEEE Transactions on NanoBioscience 6:4, pages 282-288.
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P.K. Chan, E.S.K. Ma, S. Philipsen & K.C. Tan‐Un. (2006) The study of sequence configuration and functional impact of the (AC) n (AT) x T y motif in human β‐globin gene promoter . American Journal of Hematology 82:5, pages 342-348.
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