Citations (8)
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Ahmet Genc, Deniz Tastemir Korkmaz, Suleyman Bayram & Eyyup Rencuzogullari. (2020) The Effect of Five Single Nucleotide Polymorphisms on Hb F Variation of β-Thalassemia Traits and Hematologically Normal Individuals in Southeast Turkey. Hemoglobin 44:4, pages 231-239.
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Awatef Mejri, Marwa Mansri, Sondess Hadj Fredj, Faida Ouali, Amina Bibi, Raouf Hafsia, Taieb Messaoud & Hajer Siala. (2016) First description of the rs45496295 polymorphism of the C/EBPE gene in β-thalassemia intermedia patients. Hemoglobin 40:6, pages 411-416.
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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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Mehdi Haghi, Abbas A. Hosseinpour Feizi, Cornelis L. Harteveld, Nasser Pouladi & Mohammad A. Hosseinpour Feizi. (2009) Homozygosity for a Rare β0-Thalassemia Mutation [Frameshift Codons 25/26 (+T)] Causes β-Thalassemia Intermedia in an Iranian Family. Hemoglobin 33:1, pages 75-80.
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Articles from other publishers (4)
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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Sandro Trova, Paolo Mereu, Elena Cocco, Bruno Masala, Laura Manca & Monica Pirastru. (2016) The New -474(C→T) Substitution Discovered in the <b><i>HBG2</i></b> Promoter of a Sardinian δβ-Thalassemia Carrier. Acta Haematologica 136:3, pages 178-185.
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Kais Douzi, Imen Moumni, Amine Zorai, Maha Ben Mustapha, Ikbel Mosbahi Ben Mansour, Chaouachi Dorra & Abbes Salem. (2015)
Two new β
+
-thalassemia mutation [
β -56 (G → C); HBBc. −106 G → C
] and [
β −83 (G → A); HBBc. −133 G → A
] described among the Tunisian population
. American Journal of Human Biology 27:5, pages 716-719.
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Awatef Mejri, Hajer Siala, Faida Ouali, Amina Bibi & Taieb Messaoud. (2012) Identification of candidate genes involved in clinical variability among Tunisian patients with β-thalassemia. Gene 506:1, pages 166-172.
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