Mid-Frequency Hearing Loss Is Characteristic Clinical Feature of OTOA-Associated Hearing Loss

The OTOA gene (Locus: DFNB22) is reported to be one of the causative genes for non-syndromic autosomal recessive hearing loss. The copy number variations (CNVs) identified in this gene are also known to cause hearing loss, but have not been identified in Japanese patients with hearing loss. Furtherm...

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Detalles Bibliográficos
Autores principales: Sugiyama, Kenjiro, Moteki, Hideaki, Kitajiri, Shin-ichiro, Kitano, Tomohiro, Nishio, Shin-ya, Yamaguchi, Tomomi, Wakui, Keiko, Abe, Satoko, Ozaki, Akiko, Motegi, Remi, Matsui, Hirooki, Teraoka, Masato, Kobayashi, Yumiko, Kosho, Tomoki, Usami, Shin-ichi
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2019
Materias:
Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6770988/
https://www.ncbi.nlm.nih.gov/pubmed/31527525
http://dx.doi.org/10.3390/genes10090715

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6770988/
https://www.ncbi.nlm.nih.gov/pubmed/31527525
http://dx.doi.org/10.3390/genes10090715

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