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Jan 7, 2022 (publication date) through Apr 11, 2026
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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
| 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 [PMID: 35071519 DOI: 10.12998/wjcc.v10.i1.205] |
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| ©2004-2026 Baishideng Publishing Group Inc. All rights reserved. 7041 Koll Center Parkway, Suite 160, Pleasanton, CA 94566, USA | |
| For: | 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 [PMID: 35071519 DOI: 10.12998/wjcc.v10.i1.205] |
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| URL: | https://www.wjgnet.com/2307-8960/full/v10/i1/205.htm |
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| 2 |
Nandita Sharma, Divya Kumari, Inusha Panigrahi, Preeti Khetarpal. A systematic review of the monogenic causes of Non‐Syndromic Hearing Loss (NSHL) and discussion of Current Diagnosis and Treatment options. Clinical Genetics 2023; 103(1): 16 doi: 10.1111/cge.14228
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