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.
Cite
CITATION STYLE
APA
Jennings, L. J., & Kirschmann, D. (2016). Genetic Testing Requires NGS and Sanger Methodologies. Pediatric Neurology Briefs, 30(9), 36. https://doi.org/10.15844/pedneurbriefs-30-9-1
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