Copyright
©The Author(s) 2022.
World J Clin Cases. Jan 7, 2022; 10(1): 205-216
Published online Jan 7, 2022. doi: 10.12998/wjcc.v10.i1.205
Published online Jan 7, 2022. doi: 10.12998/wjcc.v10.i1.205
Figure 2 Clinical and genetic characterization of the two Chinese families.
A: Air conduction audiogram of four subjects. Symbols: X-left, O-right ear; B: Partial sequence chromatograms of tRNAIle gene from two probands and a control subject, respectively.
- Citation: Zhao LJ, Zhang ZL, Fu Y. Novel m.4268T>C mutation in the mitochondrial tRNAIle 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