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1:1,000 dilution), anti-solute carrier family 7 member 11 (SLC7A11

Subsequently, whole exome sequencing (WES) of simplex families with one affected child demonstrated strong association of rare de novo exonic single nucleotide variants (SNV) with ASD [20,21,22,23,24], with more recent analyses highlighting around a hundred genome-wide significant ASD risk genes [25, 26]

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m , Summary of half-maximum inhibitory concentration (pIC 50 ) values of NAMs on the above constructs