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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Detalhes bibliográficos
Publicado no:Genes (Basel)
Main Authors: 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: Artigo
Idioma:Inglês
Publicado em: MDPI 2019
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Article
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC6770988/
https://ncbi.nlm.nih.gov/pubmed/31527525
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.3390/genes10090715
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