کد مقاله | کد نشریه | سال انتشار | مقاله انگلیسی | نسخه تمام متن |
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1971082 | 1059835 | 2009 | 7 صفحه PDF | دانلود رایگان |
ObjectivesLMNA mutations lead to a wide spectrum of disorders now called laminopathies. Due to large cohorts to investigate, mutational screening must be performed using an extremely sensitive and specific scanning method.Design and methodsHigh Resolution Melting (HRM) analysis was developed for LMNA mutation detection. A cohort of 64 patients with dilated cardiomyopathy was prospectively screened using both HRM and DHPLC methodologies.ResultsAll gene variants detected by DHPLC or by direct sequencing were also readily identified as abnormal by HRM analysis. Mutations were identified in 7 patients (~ 11%). Complete molecular LMNA investigation was completed two times faster and cheaper than using DHPLC strategy.ConclusionsHRM analysis represents an inexpensive, highly sensitive and high-throughput method to identify LMNA genetic variants. The discovery of novel LMNA mutations will provide new insights into the pathophysiology of dilated cardiomyopathy and in all other laminopathies.
Journal: Clinical Biochemistry - Volume 42, Issue 9, June 2009, Pages 892–898