Novel m.4268T>C mutation in the mitochondrial tRNAIle gene is associated with hearing loss in two Chinese families

doi:10.12998/wjcc.v10.i1.205

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205

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Jan 7, 2022 (publication date) through May 16, 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. Jan 7, 2022; 10(1): 205-216
Published online Jan 7, 2022. doi: 10.12998/wjcc.v10.i1.205

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Figure 1 Two Chinese families with hearing loss. An arrow denotes the proband.

Citation: Zhao LJ, Zhang ZL, Fu Y. Novel m.4268T>C mutation in the mitochondrial tRNA^Ile gene is associated with hearing loss in two Chinese families. World J Clin Cases 2022; 10(1): 205-216
URL: https://www.wjgnet.com/2307-8960/full/v10/i1/205.htm
DOI: https://dx.doi.org/10.12998/wjcc.v10.i1.205