Copyright
©The Author(s) 2021.
World J Clin Cases. Aug 16, 2021; 9(23): 6858-6866
Published online Aug 16, 2021. doi: 10.12998/wjcc.v9.i23.6858
Published online Aug 16, 2021. doi: 10.12998/wjcc.v9.i23.6858
Figure 1 Heterozygous deletion mutations found at exons 6–21 in the child as revealed by whole-exome sequencing.
Figure 2 No anomalies were found at exons 6–21 in the child’s parents as revealed by whole-exome sequencing.
- Citation: Lin SZ, Zhou XY, Wang WQ, Jiang K. Autism with dysphasia accompanied by mental retardation caused by FOXP1 exon deletion: A case report. World J Clin Cases 2021; 9(23): 6858-6866
- URL: https://www.wjgnet.com/2307-8960/full/v9/i23/6858.htm
- DOI: https://dx.doi.org/10.12998/wjcc.v9.i23.6858