Clinical Characteristics and In Vitro Analysis of MYO6 Variants Causing Late-onset Progressive Hearing Loss

MYO6 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 MYO6 gene mutations, a large-scale genetic analysis of Japanese patients with hearing loss was perform...

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Pubblicato in:Genes (Basel)
Autori principali: Oka, Shin-ichiro, Day, Timothy F., Nishio, Shin-ya, Moteki, Hideaki, Miyagawa, Maiko, Morita, Shinya, Izumi, Shuji, Ikezono, Tetsuo, Abe, Satoko, Nakayama, Jun, Hyogo, Misako, Okamoto, Nobuhiko, Uehara, Natsumi, Oshikawa, Chie, Kitajiri, Shin-ichiro, Usami, Shin-ichi
Natura: Artigo
Lingua:Inglês
Pubblicazione: MDPI 2020
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Article
Accesso online:https://ncbi.nlm.nih.gov/pmc/articles/PMC7140843/
https://ncbi.nlm.nih.gov/pubmed/32143290
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.3390/genes11030273
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