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Hemoglobin
international journal for hemoglobin research
Volume 39, 2015 - Issue 4
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Short Communication

Occurrence of the Codon 24 (A > T) Mutation in the Mauritanian Population

Fatimetou VetenUnité de Recherche sur les Biomarqueurs de la Population Mauritanienne, Faculté des Sciences et Techniques, Université des Sciences de Technologies et de Médicine, Nouakchott, Mauritanie
,
Sidi GhaberLaboratoire de Biochimie, Faculté de Médecine, Université des Sciences de Technologies et de Médicine, Nouakchott, Mauritanie
,
Nordine HabtiLaboratoire d’Hématologie et de Génie Génétique et Cellulaire, Faculté de Médecine et de Pharmacie de Casablanca, Université Hassan II Aïn Chock, Maroc
&
Ahmed HoumeidaUnité de Recherche sur les Biomarqueurs de la Population Mauritanienne, Faculté des Sciences et Techniques, Université des Sciences de Technologies et de Médicine, Nouakchott, Mauritanie Correspondence[email protected]
Pages 296-297 | Received 11 Oct 2014, Accepted 21 Dec 2014, Published online: 05 Jun 2015

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Sidi M. Ghaber, Nawel Trabelsi, Mohamed L. Salem, Faten Haddad, Aminetou Abba, Imen Darragi & Salem Abbes. (2018) Hb Moscva [β24(B6)Gly→Asp (GGT>GAT), HBB: c.74G>A]: An Unstable Hemoglobin Newly Detected as a De Novo Mutation in a Mauritanian Patient. Hemoglobin 42:1, pages 7-10.
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Gisele C.S. Carrocini, Larissa P.R. Venancio, Viviani L.R. Pessoa, Clarisse L.C. Lobo & Claudia R. Bonini-Domingos. (2017) Mutational Profile of Homozygous β-Thalassemia in Rio de Janeiro, Brazil. Hemoglobin 41:1, pages 12-15.
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Articles from other publishers (2)

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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Cheikh Tijani Hamed, Ghlana Meiloud, Fatimetou Veten, Mouna Hadrami, Sidi M. Ghaber, Ely C. Boussaty, Norddine Habti & Ahmed Houmeida. (2018) HLA class I (-A, -B, -C) and class II (-DR, -DQ) polymorphism in the Mauritanian population. BMC Medical Genetics 19:1.
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