INPLASY202520026 Decoding SCN2A Variants: Bridging Genetics and Phenotypes in Autism Spectrum Disorder Keywords: Autism Spectrum Disorder; SCN2A; Nav1.2 sodium channel; genetic mutations; neurodevelopmental disorders; genotype-phenotype correlation; de novo mutations; personalized medicine; intellectual disability. Read and download full-text here - PDF 202520026 Review Status: completed but not published
