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Sep 6, 2023 (publication date) through Apr 15, 2025
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Publication Name
World Journal of Clinical Cases
ISSN
2307-8960
Publisher of This Article
Baishideng Publishing Group Inc, 7041 Koll Center Parkway, Suite 160, Pleasanton, CA 94566, USA
| For: | Xia CF, Yan R, Su WW, Liu YH. Autosomal dominant non-syndromic hearing loss caused by a novel mutation in MYO7A: A case report and review of the literature. World J Clin Cases 2023; 11(25): 5962-5969 [PMID: 37727480 DOI: 10.12998/wjcc.v11.i25.5962] |
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| URL: | https://www.wjgnet.com/2307-8960/full/v11/i25/5962.htm |
| Number | Citing Articles |
| 1 |
Ya’nan Zhang, Xinyi Guo, Ling Hao, Meihui Tian, Yuan Ma, Yong Tang. Identification of a novel compound heterozygous pathogenic variant in MYO7A causing Usher syndrome type IB in a Chinese patient: a case report. Journal of International Medical Research 2023; 51(12) doi: 10.1177/03000605231218924
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| 2 |
Prashun Acharya, Garima Thapa, Xiayi Liao, Samaneh Matoo, Maura J. Graves, Sarah Y. Atallah, Ashna K. Tipirneni, Tram Nguyen, Niki M. Chhabra, Jaden Maschack, Mackenzie R. Herod, Favour A. Ohaezu, Alder Robison, Ashwini Mudaliyar, Jasvinder Bharaj, Nicole Roeser, Katherine Holmes, Vishwaas Nayak, Rayah Alsayed, Benjamin J. Perrin, Scott W. Crawley. Select autosomal dominant DFNA11 deafness variants activate Myo7A targeting in epithelial cells. Journal of Cell Science 2025; 138(7) doi: 10.1242/jcs.263982
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