Novel ACTG1 mutations in patients identified by massively parallel DNA sequencing cause progressive hearing loss

Human ACTG1 mutations are associated with high-frequency hearing loss, and patients with mutations in this gene are good candidates for electric acoustic stimulation. To better understand the genetic etiology of hearing loss cases, massively parallel DNA sequencing was performed on 7,048 unrelated J...

Descripción completa

Detalles Bibliográficos
Autores principales: Miyajima, Hiroki, Moteki, Hideaki, Day, Timothy, Nishio, Shin-ya, Murata, Takaaki, Ikezono, Tetsuo, Takeda, Hidehiko, Abe, Satoko, Iwasaki, Satoshi, Takahashi, Masahiro, Naito, Yasushi, Yamazaki, Hiroshi, Kanda, Yukihiko, Kitajiri, Shin-ichiro, Usami, Shin-ichi
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2020
Materias:
Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7184572/
https://www.ncbi.nlm.nih.gov/pubmed/32341388
http://dx.doi.org/10.1038/s41598-020-63690-5

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7184572/
https://www.ncbi.nlm.nih.gov/pubmed/32341388
http://dx.doi.org/10.1038/s41598-020-63690-5

Ejemplares similares