Copyright
©The Author(s) 2021.
World J Clin Cases. Nov 26, 2021; 9(33): 10257-10264
Published online Nov 26, 2021. doi: 10.12998/wjcc.v9.i33.10257
Published online Nov 26, 2021. doi: 10.12998/wjcc.v9.i33.10257
Figure 2 Sanger sequencing of the patient and his parent’s DNA samples.
A: The reference corresponding DNA sequences of KDM6A gene from the NCBI GenBank; B: DNA sequence of the DNA sample from the patient. The DNA sequencing data demonstrated AG deletion (chr23:44911001_44911002delAG, c.702_703delAG, p. N236Sfs*26); C, D: DNA sequence of the samples from his parents. The data showed no KDM6A gene mutation.
- Citation: Guo HX, Li BW, Hu M, Si SY, Feng K. Novel KDM6A mutation in a Chinese infant with Kabuki syndrome: A case report. World J Clin Cases 2021; 9(33): 10257-10264
- URL: https://www.wjgnet.com/2307-8960/full/v9/i33/10257.htm
- DOI: https://dx.doi.org/10.12998/wjcc.v9.i33.10257