A MYT1L syndrome mouse model recapitulates patient phenotypes and reveals altered brain development due to disrupted neuronal maturation

It has come to our attention that the S710fsX mutation of our MYT1L mice is actually on exon 11 instead of 7, as stated in our published paper. We tracked the error to a truncated file used for annotation at the very beginning of the project. There are three places we mentioned “Exon 7,” including two in the main text and one in Figure 1. These should instead read “Exon 11.” The information on the consequences of the mutation is otherwise correct. We, the authors, apologize for the error.