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CHAPEL HILL - Scientists at the University of North Carolina at Chapel Hill School of Medicine and colleagues have demonstrated that rare variants in
Scientists suggest new insights, tools, and methods will help to assign pathogenicity to other ANK2 variants.
Scientists at the University of North Carolina at Chapel Hill School of Medicine and colleagues have demonstrated that rare variants in the ANK2 gene, consistently found in individuals with autism spectrum disorder (ASD), can alter architecture and organization of neurons, potentially contributing to autism and neurodevelopmental comorbidities.
Scientists have demonstrated that rare variants in the <i>ANK2</i> gene, consistently found in individuals with autism spectrum disorder (ASD), can alter the architecture and organization of neurons, potentially contributing to autism and neurodevelopmental comorbidities.
Scientists at the University of North Carolina at Chapel Hill School of Medicine and colleagues have demonstrated that rare variants in the ANK2 gene