Exome & General Genetics

Session # 2910W ‡

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

Reviewers' Choice Abstracts

  • Authors: Deepali Shinde; L. Rohena; S. Weatherspoon; Katherine Helbig; Christian Antolik; D.R. Hamlin; J.M. Berg; Schul; Catherine Schultz; Zöe Powis; Sha Tang; Kelly Radtke
  • Collaborators: Children's Hospital of Philadelphia; The University of Texas
  • Conference: American Society of Human Genetics (ASHG) 2018
  • Date: Wednesday, Oct 17, 2018 3:00am - 4:00pm

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