کد مقاله | کد نشریه | سال انتشار | مقاله انگلیسی | نسخه تمام متن |
---|---|---|---|---|
1970805 | 1538901 | 2009 | 10 صفحه PDF | دانلود رایگان |

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.
Journal: Clinical Biochemistry - Volume 42, Issues 16–17, November 2009, Pages 1667–1676