Clinical and genetic study of ataxia with vitamin E deficiency: A case report

doi:10.12998/wjcc.v10.i23.8271

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Aug 16, 2022 (publication date) through May 11, 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. Aug 16, 2022; 10(23): 8271-8276
Published online Aug 16, 2022. doi: 10.12998/wjcc.v10.i23.8271

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Figure 1 Pedigree and sanger sequencing validation of homozygous mutation c. 473T>C, p.F158S of TTPA gene in this pedigree. Clear square: Male; Clear circle: Female; Black circle: Index patient.

Citation: Zhang LW, Liu B, Peng DT. Clinical and genetic study of ataxia with vitamin E deficiency: A case report. World J Clin Cases 2022; 10(23): 8271-8276
URL: https://www.wjgnet.com/2307-8960/full/v10/i23/8271.htm
DOI: https://dx.doi.org/10.12998/wjcc.v10.i23.8271