Copyright
©The Author(s) 2023.
World J Clin Cases. Apr 6, 2023; 11(10): 2254-2259
Published online Apr 6, 2023. doi: 10.12998/wjcc.v11.i10.2254
Published online Apr 6, 2023. doi: 10.12998/wjcc.v11.i10.2254
Figure 1 Sanger sequencing results of the ABCC8 gene in the child, his sister, and his parents.
A c.1257 mutation (thymine displacement in coding region no. 1257) occurred in the ABCC8 gene in the child and his sister. The mutation derived from the patient’s mother.
- Citation: Liu MT, Yang HX. Neonatal hyperinsulinism with an ABCC8 mutation: A case report. World J Clin Cases 2023; 11(10): 2254-2259
- URL: https://www.wjgnet.com/2307-8960/full/v11/i10/2254.htm
- DOI: https://dx.doi.org/10.12998/wjcc.v11.i10.2254