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Ahsan Hussain, Suhaib Ahmed, Nadir Ali, Hamid S. Mailk, Mariam Anees, Altaf H. Chuahdry & Parvez Ahmed. (2017) Rare β-Globin Gene Mutations in Pakistan. Hemoglobin 41:2, pages 100-103.
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Sevcan Tug Bozdogan, Cagatay Unsal, Hakan Erkman, Ahmet Genc, Ozge Ozalp Yuregir, Muhammed Hamza Muslumanoglu & Huseyin Aslan. (2012) Nonsense β-Thalassemia Mutation at Codon 37 (TGG>TGA), Detected for the First Time in Three Turkish Cases. Hemoglobin 36:3, pages 283-288.
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Alice E. Gallienne, Nicola M. Iberson, Hélène M. Dréau, Helen Jackson, Patricia A. Bignell, John M. Old, Anna Schuh & Shirley J. Henderson. (2010) Characterization of a Novel Deletion Causing β-Thalassemia Major in an Afghan Family. Hemoglobin 34:1, pages 110-114.
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Dongzhi Li, Can Liao, Jian Li & Xuewei Tang. (2006) The Codon 37 (TGG→TAG) β0-Thalassemia Mutation Found in a Chinese Family. Hemoglobin 30:2, pages 171-173.
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Articles from other publishers (6)
Opeyemi S. Soremekun, Chisom Ezenwa, Itunuoluwa Isewon, Mahmoud Soliman, Omotuyi Idowu, Oyekanmi Nashiru & Segun Fatumo. (2020) Computational and drug target analysis of functional single nucleotide polymorphisms associated with Haemoglobin Subunit Beta (HBB) gene. Computers in Biology and Medicine 125, pages 104018.
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Jinliang Yang, Jian Lian, Haitao Pu & Jason Gu. (2017) Modeling and analysis of DNA mutation type based on colored Petri net. Modeling and analysis of DNA mutation type based on colored Petri net.
Jinliang Yang, Rui Gao, Max Q.-H. Meng & Tzyh-Jong Tarn. (2012) Colored petri nets to model gene mutation and amino acids classification. Journal of Theoretical Biology 300, pages 183-192.
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Francesca Salvatori, Giulia Breveglieri, Cristina Zuccato, Alessia Finotti, Nicoletta Bianchi, Monica Borgatti, Giordana Feriotto, Federica Destro, Alessandro Canella, Eleonora Brognara, Ilaria Lampronti, Laura Breda, Stefano Rivella & Roberto Gambari. (2009)
Production of β‐globin and adult hemoglobin following G418 treatment of erythroid precursor cells from homozygous β
0
39 thalassemia patients
. American Journal of Hematology 84:11, pages 720-728.
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Francesca Salvatori, Vera Cantale, Giulia Breveglieri, Cristina Zuccato, Alessia Finotti, Nicoletta Bianchi, Monica Borgatti, Giordana Feriotto, Federica Destro, Alessandro Canella, Laura Breda, Stefano Rivella & Roberto Gambari. (2009)
Development of K562 cell clones expressing β-globin mRNA carrying the β
0
39 thalassaemia mutation for the screening of correctors of stop-codon mutations
. Biotechnology and Applied Biochemistry 54:1, pages 41-52.
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C Préhu, J Riou, J Henthorn & H Wajcman. (2007) A New Silent β Chain Variant: Hb Hounslow [β80(EF4)Asn→Tyr]. Balkan Journal of Medical Genetics 10:1, pages 29-32.
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