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Hemoglobin
international journal for hemoglobin research
Volume 30, 2006 - Issue 2
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SHORT COMMUNICATION

The Codon 37 (TGG→TAG) β0-Thalassemia Mutation Found in a Chinese Family

Dongzhi Li Prenatal Diagnostic Center, Guangzhou Maternal & Neonatal Hospital, Guangzhou Medical College, Guangzhou, Guangdong, People's Republic of ChinaCorrespondence[email protected]
,
Can Liao Prenatal Diagnostic Center, Guangzhou Maternal & Neonatal Hospital, Guangzhou Medical College, Guangzhou, Guangdong, People's Republic of China
,
Jian Li Prenatal Diagnostic Center, Guangzhou Maternal & Neonatal Hospital, Guangzhou Medical College, Guangzhou, Guangdong, People's Republic of China
&
Xuewei Tang Prenatal Diagnostic Center, Guangzhou Maternal & Neonatal Hospital, Guangzhou Medical College, Guangzhou, Guangdong, People's Republic of China
Pages 171-173 | Received 06 Sep 2005, Accepted 28 Oct 2005, Published online: 07 Jul 2009

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Read on this site (2)

Fan Jiang, Lv-Yin Huang, Gui-Lan Chen, Jian-Ying Zhou, Xing-Mei Xie & Dong-Zhi Li. (2017) A Novel Frameshift Mutation at Codons 138/139 (HBB: c.417_418insT) on the β-Globin Gene Leads to β-Thalassemia. Hemoglobin 41:1, pages 59-60.
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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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Articles from other publishers (4)

R. Angalena, K. N. Prabitha, A. K. Chaudhary, M. D. Bashyam, S. Jain & A. B. Dalal. (2010) LETTER TO THE EDITOR: A novel homozygous point mutation at codon 82 (HBB:c.247A > T) in the beta‐globin gene leads to thalassemia major. International Journal of Laboratory Hematology 32:5, pages 548-549.
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Dong-Zhi Li, Can Liao, Jian Li & Ru Li. (2009) A novel β-globin gene deletion (codons 89–93) in a Chinese family. Annals of Hematology 89:3, pages 323-325.
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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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