The Human Neurogenetics team has produced the first knok-in model of severe neonatal epilepsy caused by Kcnq2. The model is now published in Epilepsia, and it will allow a better understanding of Kcnq2 related epileptic encephalopathy, and will be a relevant tool to test new therapeutic approaches.
The paper is published as open access:
https://www.ncbi.nlm.nih.gov/pubmed/32239694