Genetic Testing Requires NGS and Sanger Methodologies

Jennings, L. J.; Kirschmann, D.

Pediatr Neurol Briefs. 2016 Sep 22; 30(9):36

Abstract

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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