What can be understood from a single audiogram “Case presentation from a university hospital”
Author:
Affiliation:
1. Department of Otorhinolaryngology, International University of Health and Welfare, Mita hospital
Publisher
Japan Audiological Society
Link
https://www.jstage.jst.go.jp/article/audiology/67/3/67_188/_pdf
Reference15 articles.
1. 1) Usami S, Nishio SY: The genetic etiology of hearing loss in Japan revealed by the social health insurance-based genetic testing of 10K patients. Hum Genet 141: 665-681, 2022
2. 2) Miyagawa M, Nishio SY, Ichinose A, et al: Mutational spectrum and clinical features of hearing loss with ACTG1 mutations identified by massively parallel DNA sequencing. Ann Otol Rhinol Laryngo 124 (Suppl 1): 84S-93S, 2015
3. 3) Miyagawa M, Nishio SY, Usami S, et al: Prevalence and clinical features of hearing loss patients with CDH23 mutations: a large cohort study. Plos One 7: e40366, 2012
4. 4) Tsukada K, Ichinose A, Miyagawa M, et al: Detailed hearing and vestibular profiles in the patients with COCH mutations. Ann Otol Rhinol Laryngo 124 (Suppl 1): 100S-10S, 2015
5. 5) Naito T, Nishio SY, Iwasa Y, et al: Comprehensive genetic screening of KCNQ4 in a large autosomal dominant nonsyndromic hearing loss cohort: genotype-phenotype correlations and a founder mutation. PLos One 8: e63231, 2013
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