Genetic Testing Requires NGS and Sanger Methodologies.
Pediatric neurology briefs(2016)
摘要
Investigators from the EuroEPINOMICS rare epilepsy syndromes Dravet working group performed whole-exome sequencing on 31 trios that had been reported negative for SCN1A mutations by Sanger sequencing.
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关键词
NGS,SCN1A,Sanger
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