Fig. 1From: Heterozygous deletion of SCN2A and SCN3A in a patient with autism spectrum disorder and Tourette syndrome: a case reportResults of microarray-analysis. Molecular karyotyping revealed a deletion of approximately 719 kb out of the chromosomal region 2q24.3 encompassing the 5 genes GRB14 (exon 1 to intron 2–3), COBLL1, SLC38A11, SCN3A and SCN2A (exon 1 to intron 14–15) listed in OMIM (Online Mendelian Inheritance in Man)Back to article page