Citations (23)
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Maria Ascensión Herrera, Félix De La Fuente-Gonzalo, Fernando Ataúlfo González, Jorge M. Nieto, Alejandra Blum Dominguez, Ana Villegas & Paloma Ropero. (2015) Identification of a Novel Mutation in the β-Globin Gene 3′ Untranslated Region (HBB: c.*+118A > G) in Spain. Hemoglobin 39:1, pages 30-35.
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Articles from other publishers (10)
Adivitch Sripusanapan, Arunee Phusua, Kanda Fanhchaksai & Pimlak Charoenkwan. (2020)
Compound heterozygosity of a silent beta‐thalassemia mutation at the 3′‐untranslated region (
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M. Vinciguerra, C. Passarello, F. Cassarà, F. Leto, M. Cannata, G. Calvaruso, R. Di Maggio, D. Renda, A. Maggio & A. Giambona. (2016)
Co-heredity of silent CAP + 1570 T>C (
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Jian-Min Chen, Claude Férec & David N. Cooper. (2006) A systematic analysis of disease-associated variants in the 3′ regulatory regions of human protein-coding genes II: the importance of mRNA secondary structure in assessing the functionality of 3′ UTR variants. Human Genetics 120:3, pages 301-333.
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Onur Bilenoglu, A. Nazli Basak & J. Eric Russell. (2002) A 3′UTR mutation affects β‐globin expression without altering the stability of its fully processed mRNA. British Journal of Haematology 119:4, pages 1106-1114.
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Argyro Sgourou, Adamandia Papachatzopoulou, Lambrini Psiouri, Michael Antoniou, Nicholas Zoumbos, Richard Gibbs & Aglaia Athanassiadou. (2002) The β-globin C→G mutation at 6 bp 3′ to the termination codon causes β-thalassaemia by decreasing the mRNA level. British Journal of Haematology 118:2, pages 671-676.
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G.O. Tadmouri, Ş. Tüzmen, H. Özçelik, A. Özer, S.M. Baig, E.B. Senga & A.N. Başak. (1998) Molecular and population genetic analyses of β-Thalassemia in Turkey. American Journal of Hematology 57:3, pages 215-220.
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