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Study reveals how genetic changes in SCN2A gene impact autism and epilepsy

A genetic change or variant in a gene called SCN2A is a known cause of infantile seizures, autism spectrum disorder and intellectual disability, as well as a wide range of other moderate-to-profound impairments in mobility, communication, eating and vision.

Vitiglio Patients Share Their Treatment Frustrations With FDA

Vitiglio Patients Share Their Treatment Frustrations With FDA
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