Genetic Testing Requires NGS and Sanger Methodologies

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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Bibliographic Details
Main Authors: Lawrence J. Jennings (Author), Dawn Kirschmann (Author)
Format: Book
Published: Pediatric Neurology Briefs Publishers, 2016-09-01T00:00:00Z.
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3rd Floor Main Library

Holdings details from 3rd Floor Main Library
Call Number: A1234.567
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