Copyright
©The Author(s) 2023.
World J Clin Cases. Apr 16, 2023; 11(11): 2452-2456
Published online Apr 16, 2023. doi: 10.12998/wjcc.v11.i11.2452
Published online Apr 16, 2023. doi: 10.12998/wjcc.v11.i11.2452
Figure 1 Whole-exome gene sequencing.
A: IFIH1 gene of the patient was found to have c.1093A>G (p.Lys365Glu), and heterozygous mutation. B: The source of mutation was her father. C: The sequencing of the patient’s mother.
- Citation: Lin SZ, Yang JJ, Xie TL, Li JY, Ma JQ, Wu S, Wang N, Wang YJ. Aicardi-Goutières syndrome type 7 in a Chinese child: A case report. World J Clin Cases 2023; 11(11): 2452-2456
- URL: https://www.wjgnet.com/2307-8960/full/v11/i11/2452.htm
- DOI: https://dx.doi.org/10.12998/wjcc.v11.i11.2452