Prevalence and clinical features of hearing loss caused by EYA4 variants

Variants in the EYA4 gene are known to lead to autosomal dominant non-syndromic hereditary hearing loss, DFNA10. To date, 30 variants have been shown to be responsible for hearing loss in a diverse set of nationalities. To better understand the clinical characteristics and prevalence of DFNA10, we p...

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Detaylı Bibliyografya
Yayımlandı:Sci Rep
Asıl Yazarlar: Shinagawa, Jun, Moteki, Hideaki, Nishio, Shin-ya, Ohyama, Kenji, Otsuki, Koshi, Iwasaki, Satoshi, Masuda, Shin, Oshikawa, Chie, Ohta, Yumi, Arai, Yasuhiro, Takahashi, Masahiro, Sakuma, Naoko, Abe, Satoko, Sakurai, Yuika, Sakaguchi, Hirofumi, Ishino, Takashi, Uehara, Natsumi, Usami, Shin-ichi
Materyal Türü: Artigo
Dil:Inglês
Baskı/Yayın Bilgisi: Nature Publishing Group UK 2020
Konular:
Article
Online Erişim:https://ncbi.nlm.nih.gov/pmc/articles/PMC7046659/
https://ncbi.nlm.nih.gov/pubmed/32107406
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1038/s41598-020-60259-0
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