Novel mutation in the ASXL3 gene in a Chinese boy with microcephaly and speech impairment: A case report

doi:10.12998/wjcc.v8.i24.6465

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Dec 26, 2020 (publication date) through May 17, 2024

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World Journal of Clinical Cases

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2307-8960

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Baishideng Publishing Group Inc, 7041 Koll Center Parkway, Suite 160, Pleasanton, CA 94566, USA

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World J Clin Cases. Dec 26, 2020; 8(24): 6465-6472
Published online Dec 26, 2020. doi: 10.12998/wjcc.v8.i24.6465

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Figure 1 Pictures of our patient at age 3 years. A-C: Facial characteristics; D: Dental abnormalities; E and F: Hands.

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