A novel β-globin gene deletion (codons 89–93) in a Chinese family
Author:
Publisher
Springer Science and Business Media LLC
Subject
Hematology,General Medicine
Link
http://link.springer.com/content/pdf/10.1007/s00277-009-0798-3.pdf
Reference13 articles.
1. Xu XM, Zhou YQ, Luo GX et al (2004) The prevalence and spectrum of α- and β-thalassemia in Guangdong Province: implications for the future health burden and population screening. J Clin Pathol 57:517–522
2. Li DZ, Liao C, Xie XM, Zhou JY (2009) A novel mutation of −50 (G→A) in the direct repeat element of the β-globin gene identified in a patient with severe β-thalassemia. Ann Hematol (in press). doi: 10.1007/s00277-009-0732-8
3. Li DZ, Liao C, Li J (2009) A novel β-thalassemic allele due to a thirteen nucleotide deletion: codons 54–58 (−T ATG GGC AAC CCT). Ann Hematol 88:799–801
4. Liao C, Li DZ, Li J (2008) First detection of the codons 41–43 (−CTTTG, +A) β-thalassemia mutation in a Chinese patient. Ann Hematol 87:775–776
5. Li D, Liao C, Li J, Tang X (2006) The codon 37 (TGG→TAG) β(0)-thalassemia mutation found in a Chinese family. Hemoglobin 30:171–173
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4. A Novel Frameshift Mutation at Codons 138/139 (HBB: c.417_418insT) on the β-Globin Gene Leads to β-Thalassemia;Hemoglobin;2017-01-02
5. Identification of a Novel β-Globin Mutation (HBB: C.189_195delTCATGGC) in a Chinese Family;Hemoglobin;2016-07-03
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