Article ID Journal Published Year Pages File Type
1970805 Clinical Biochemistry 2009 10 Pages PDF
Abstract

ObjectiveThis study was undertaken to identify HBB gene mutation.Design and methodsHerein we evaluated high-resolution melting analysis in the identification of HBB mutations.ResultsWe have successfully established a diagnostic strategy for identifying HBB gene mutations including c.− 78A > G, c.− 79A > G, c.2T > G, c.79_80insT, c.84_85insC, c.123_124insT, c.125_128delTCTT, c.130 G > T, c.170G > A, c.216_217ins A and c.316–197 C > T from wild-type DNA using HRM analysis. The results of HRM analysis were confirmed by direct DNA sequencing.ConclusionsIn summary, we report that HRM analysis is an appealing technique for the identification of HBB mutations. We also believe that HRM can be used as a method for prenatal diagnosis of β-thalassemia.

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Life Sciences Biochemistry, Genetics and Molecular Biology Biochemistry
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