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Hemoglobin
international journal for hemoglobin research
Volume 34, 2010 - Issue 6
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Original Article

Coinheritance of α-Thalassemia Decreases the Risk of Cerebrovascular Disease in a Cohort of Children with Sickle Cell Anemia

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Pages 516-529 | Received 08 May 2010, Accepted 08 Sep 2010, Published online: 15 Nov 2010

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Fatou Gueye Tall, Cyril Martin, El Hadji Malick Ndour, Indou Déme Ly, Céline Renoux, Louis Chillotti, Nicolas Veyrenche, Philippe Connes, Papa Madieye Gueye, Rokhaya Ndiaye Diallo, Philippe Lacan, Ibrahima Diagne, Pape Amadou Diop, Aynina Cissé, Philomène Lopez Sall & Philippe Joly. (2017) Genetic Background of the Sickle Cell Disease Pediatric Population of Dakar, Senegal, and Characterization of a Novel Frameshift β-Thalassemia Mutation [HBB: c.265_266del; p.Leu89Glufs*2]. Hemoglobin 41:2, pages 89-95.
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Renata A. Volpe de Souza, Aline Menezes Carlos, Bruna M. Bereta de Souza, Cibele Velloso Rodrigues, Gilberto de Araujo Pereira & Helio Moraes-Souza. (2015) α-Thalassemia: Genotypic Profile Associated with Ethnicity and Hematological Differentiation of Iron Deficiency Anemia in the Region of Uberaba, Minas Gerais, Brazil. Hemoglobin 39:4, pages 264-269.
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Brian M. Erazo, Gilberto A. Ramírez, Linda E. Cerrato, Luis J. Pinto, Edder J. Castro, Néstor J. Yanez, Brayan Montoya & Gustavo A. Fontecha. (2015) Prevalence of Hb S (HHB: c.20A > T) in a Honduran Population of African Descent. Hemoglobin 39:2, pages 134-137.
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