Description
“Autism has long been a hot topic of debate amongst the healthcare community and beyond. Explore the correlation of SCN2A syndromes as they relate to higher rates of autism. Most cases of autism tend to be multifactorial and complicated, but this article explores the SCN2A as a rarer monogenic etiology of disease.
SCN2A encodes the voltage gated channel Nav1.2, and has been shown to be one of the most prevalent monogenic etiologies of autism-causing mutations”.
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