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De novo missense variants in the alternative exon 5 of SCN2A are a rare cause of neurodevelopmental disorders with or without seizures

Session:
#2910
Date:
Wednesday, Oct 17, 2018 3:00am – 4:00pm
Conference:
ASHG 2018
Authors:
Catherine Schultz, Christian Antolik, D.R. Hamlin, Deepali Shinde, J.M. Berg, Katherine Helbig, Kelly Radtke, L. Rohena, S. Weatherspoon, Schul, Sha Tang, Zöe Powis
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