Article

Variants in CDH23 Cause Broad Spectrum of Hearing Loss: From Non-Syndromic to Syndromic Hearing Loss as Well as From Congenital to Age-Related Hearing Loss

2021-06-28

Abstract excerpt

<title>Abstract</title> Variants in the <italic>CDH23 </italic>gene are known to be responsible for both syndromic hearing loss (Usher syndrome type ID: USH1D) and non-syndromic hearing loss (DFNB12). Our series of studies demonstrated that <italic>CDH23 </italic>variants cause broad phenotypes of non-syndromic hearing loss (DFNB12); from congenital profound hearing loss to late-onset high frequency-involved p...

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Literature Corpus work: 9b141d90-543e-5df6-bbdb-04144fc9abdf
DOI: 10.21203/rs.3.rs-630480/v1

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