[PDF][PDF] Modelling Dravet syndrome with human iPSC-derived neural circuits
F Riccio - 2023 - kclpure.kcl.ac.uk
Dravet syndrome is a rare form of severe epilepsy primarily caused by loss-of-function
mutations of the SCN1A gene. This gene encodes for the α1-subunit of the voltage-gated …
mutations of the SCN1A gene. This gene encodes for the α1-subunit of the voltage-gated …