Copyright
©The Author(s) 2020.
World J Clin Cases. Dec 26, 2020; 8(24): 6465-6472
Published online Dec 26, 2020. doi: 10.12998/wjcc.v8.i24.6465
Published online Dec 26, 2020. doi: 10.12998/wjcc.v8.i24.6465
Figure 2 Family pedigree (the proband is marked with black arrow) and Sanger sequencing diagram of the ASXL3 variant (c.
1795G>T, p.E599*). The red arrows indicate the substitution present in the patient (A) but absent from his father (B) and mother (C).
- Citation: Li JR, Huang Z, Lu Y, Ji QY, Jiang MY, Yang F. Novel mutation in the ASXL3 gene in a Chinese boy with microcephaly and speech impairment: A case report. World J Clin Cases 2020; 8(24): 6465-6472
- URL: https://www.wjgnet.com/2307-8960/full/v8/i24/6465.htm
- DOI: https://dx.doi.org/10.12998/wjcc.v8.i24.6465