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Cited by in CrossRef
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]
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 reportJournal of International Medical Research 2023; 51(12) doi: 10.1177/03000605231218924