Clinical Characteristics and In Vitro Analysis of <i>MYO6</i> Variants Causing Late-Onset Progressive Hearing Loss

Clinical Characteristics and In Vitro Analysis of <i>MYO6</i> Variants Causing Late-Onset Progressive Hearing Loss

<i>MYO6</i> is known as a genetic cause of autosomal dominant and autosomal recessive inherited hearing loss. In this study, to clarify the frequency and clinical characteristics of hearing loss caused by <i>MYO6</i> gene mutations, a large-scale genetic analysis of Japanese...

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Bibliographic Details
Main Authors: Shin-ichiro Oka, Timothy F. Day, Shin-ya Nishio, Hideaki Moteki, Maiko Miyagawa, Shinya Morita, Shuji Izumi, Tetsuo Ikezono, Satoko Abe, Jun Nakayama, Misako Hyogo, Nobuhiko Okamoto, Natsumi Uehara, Chie Oshikawa, Shin-ichiro Kitajiri, Shin-ichi Usami
Format: Article
Language:English
Published: MDPI AG 2020-03-01
Series:Genes
Subjects:
<i>myo6</i>
myosin
non-syndromic hearing loss
dfna22
dfnb37
autosomal dominant
prevalence
genotype–phenotype correlation
hearing progression
Online Access:https://www.mdpi.com/2073-4425/11/3/273

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https://www.mdpi.com/2073-4425/11/3/273

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