Heterozygous and homozygous variants in STX1A cause a neurodevelopmental disorder with or without epilepsy
Article in European Journal of Human Genetics (December 2022)
The most recent citing publications are shown below. View all 21 publications that cite this research output on Dimensions.
Article in European Journal of Human Genetics (December 2022)
Article in CNS Neuroscience & Therapeutics (June 2022)
Preprint in medRxiv (April 2022)