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

Imane Agouti Laboratoire de Biologie Appliquée, Faculté des Sciences et Techniques, Tanger, MarocCorrespondence[email protected]

Mohcine Bennani Laboratoire de Biologie Appliquée, Faculté des Sciences et Techniques, Tanger, Maroc

Nicolas Levy Centre d'Enseignement et de Recherche en Génétique Médicale, Unité INSERM U 910, Faculté de Médecine, Marseille, France

Piero Giordano The Hemoglobinopathies Laboratory, Leiden University Medical Center, Leiden, the Netherlands

Catherine Badens Centre d'Enseignement et de Recherche en Génétique Médicale, Unité INSERM U 910, Faculté de Médecine, Marseille, France

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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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Fatimetou Veten, Sidi Ghaber, Nordine Habti & Ahmed Houmeida. (2015) Occurrence of the Codon 24 (A > T) Mutation in the Mauritanian Population. Hemoglobin 39:4, pages 296-297.
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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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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

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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

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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