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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Veröffentlicht in:Genes (Basel)
Hauptverfasser: 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
Format: Artigo
Sprache:Inglês
Veröffentlicht: MDPI 2019
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Article
Online Zugang: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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