Matt Hancock #actionforaccess #epilepsy #scn2auk #geneticepilepsy

It's time to move forward with research. Treat the disease, not manage the symptoms #scn2auk #raredisease. #scn2a #geneticepilepsy

Homozygous SCN2A gene mutation causing early infantile epileptic encephalopathy: The second case in literature | Medical Science and Discovery medscidiscovery.com/index.php/msd/… #epilepsy #SCN2AUK #raredisease #geneticepilepsy

Jayne Spink Natasha Fox (Cotter) Genetic Alliance UK #geneticepilepsy #curescn2a #scn2auk