The SCN8A interactive website makes available important information about the clinical features, causes, and treatments of SCN8A epileptic encephalopathy to families, doctors, and researchers. The website houses and curates information on clinical variability, genetic variants, anti-epileptic drugs, and current research findings associated with SCN8A epileptic encephalopathy. The purpose is to help advance SCN8A research and speed the pace of translating discoveries in the laboratory to benefit children, families, and doctors.
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