SCN2A Australia is developing a series of webinars on SCN2A, genetic epilepsy and developmental and epileptic encephalopathies (DEE).
On this page you will find links to past webinars including complete recordings, and details about upcoming webinars.
Mutations of the SCN2A gene can result in a range of different clinical syndromes. Understanding these clinical presentations can help to guide treatment.
Prof Steven Petrou and Dr Kiran Reddy discuss the RC-222 program developing an ASO treatment for gain-of-function SCN2A epilepsies.