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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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Articles from other publishers (9)
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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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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.
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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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