Article

Prevalence and Clinical Features of Autosomal Dominant and Recessive TMC1-Associated Hearing Loss.

2021-06-04

Abstract excerpt

<title>Abstract</title> <p><italic>TMC1</italic> is a causative gene for both autosomal dominant non-syndromic hearing loss (DFNA36) and autosomal recessive non-syndromic hearing loss (DFNB7/11). To date, 125 pathogenic variants in <italic>TMC1</italic> have been reported. Most of the <italic>TMC1</italic> variants are responsible for autosomal recessive hearing loss, with only 7 variants reported as causative fo...

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Literature Corpus work: 637f546b-823c-5193-8241-30b546971676
DOI: 10.21203/rs.3.rs-581891/v1

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