Genetic Testing Requires NGS and Sanger Methodologies

• मुख्य लेखकों: Lawrence J. Jennings (लेखक), Dawn Kirschmann (लेखक)
• स्वरूप: पुस्तक
• प्रकाशित: Pediatric Neurology Briefs Publishers, 2016-09-01T00:00:00Z.
• विषय: article
• ऑनलाइन पहुंच: Connect to this object online.

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.