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Our series of studies demonstrated that\n                    <jats:italic>CDH23<\/jats:italic>\n                    variants cause a\u00a0broad range of phenotypes of non-syndromic hearing loss (DFNB12); from congenital profound hearing loss to late-onset high-frequency-involved progressive hearing loss. In this study, based on the genetic and clinical data from more than 10,000 patients, the mutational spectrum, clinical characteristics and genotype\/phenotype correlations were evaluated. The present results reconfirmed that the variants in\n                    <jats:italic>CDH23<\/jats:italic>\n                    are an important cause of non-syndromic sensorineural hearing loss. In addition, we showed that the mutational spectrum in the Japanese population, which is probably representative of the East Asian population in general, as well as frequent\n                    <jats:italic>CDH23<\/jats:italic>\n                    variants that might be due to some founder effects. The present study demonstrated\n                    <jats:italic>CDH23<\/jats:italic>\n                    variants cause a broad range of phenotypes, from non-syndromic to syndromic hearing loss as well as from congenital to age-related hearing loss. Genotype (variant combinations) and phenotype (association with retinal pigmentosa, onset age) are shown to be well correlated and are thought to be related to the residual function defined by the\n                    <jats:italic>CDH23<\/jats:italic>\n                    variants.\n                  <\/jats:p>","DOI":"10.1007\/s00439-022-02431-2","type":"journal-article","created":{"date-parts":[[2022,1,12]],"date-time":"2022-01-12T11:02:38Z","timestamp":1641985358000},"page":"903-914","update-policy":"https:\/\/doi.org\/10.1007\/springer_crossmark_policy","source":"Crossref","is-referenced-by-count":47,"title":["Variants in CDH23 cause a broad spectrum of hearing loss: from non-syndromic to syndromic hearing loss as well as from congenital to age-related hearing loss"],"prefix":"10.1007","volume":"141","author":[{"ORCID":"https:\/\/orcid.org\/0000-0002-5068-6122","authenticated-orcid":false,"given":"Shin-ichi","family":"Usami","sequence":"first","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Yuichi","family":"Isaka","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Maiko","family":"Miyagawa","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Shin-ya","family":"Nishio","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]}],"member":"297","published-online":{"date-parts":[[2022,1,12]]},"reference":[{"key":"2431_CR1","doi-asserted-by":"crossref","first-page":"20070","DOI":"10.1073\/pnas.2009628117","volume":"117","author":"A Abu Rayyan","year":"2020","unstructured":"Abu Rayyan A, Kamal L, Casadei S et al (2020) Genomic analysis of inherited hearing loss in the Palestinian population. 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