Article title: Mutation in SNAP25 as a novel genetic cause of epilepsy and intellectual disability
Authors: Luis Rohena, Julie Neidich, Megan Truitt Cho, Kelly DF Gonzalez, Sha Tang, Orrin Devinsky, and Wendy Chung
Journal: Rare Diseases
Bibliometrics: Volume 1, Issue 1, e26314-1–e26314-6
DOI: 10.4161/rdis.26314
It has come to our attention that two mutations were reported in this article.
In the abstract and on page 3, it states that the mutation in SNAP25 is “p.Phe48Val.” This should be substituted with the correct mutation: “p.V48F.” as it appears in the rest of the article.
The authors apologize for any inconvenience caused.