Corrigendum to “Neurodevelopmental disorder associated with de novo SCN3A pathogenic variants: Two new cases and review of the literature” [Brain Dev. 42(2) (2020) 211–216]

Abstract

The authors regret the error below:1. Case Report -second paragraph -Whole exome sequencing (WES) SCN3A [c.5265G>A ENST00000360093, p.(Met1765Ile)] -the correct is: c.5295G>A.The authors would like to apologise for any inconvenience caused.