De novo mutation loci and clinical analysis in a child with sodium taurocholate cotransport polypeptide deficiency: A case report

doi:10.12998/wjcc.v9.i36.11487

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Dec 26, 2021 (publication date) through May 5, 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, 2021; 9(36): 11487-11494
Published online Dec 26, 2021. doi: 10.12998/wjcc.v9.i36.11487

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Figure 1 Sanger sequencing of the SLC10A1 gene of the child and parents. A: Child; B: Father; C: Mother.

Citation: Liu HY, Li M, Li Q. De novo mutation loci and clinical analysis in a child with sodium taurocholate cotransport polypeptide deficiency: A case report. World J Clin Cases 2021; 9(36): 11487-11494
URL: https://www.wjgnet.com/2307-8960/full/v9/i36/11487.htm
DOI: https://dx.doi.org/10.12998/wjcc.v9.i36.11487