Simultaneous Screening of Multiple Mutations by Invader Assay Improves Molecular Diagnosis of Hereditary Hearing Loss: A Multicenter Study

Although etiological studies have shown genetic disorders to be a common cause of congenital/early-onset sensorineural hearing loss, there have been no detailed multicenter studies based on genetic testing. In the present report, 264 Japanese patients with bilateral sensorineural hearing loss from 3...

Descripción completa

Detalles Bibliográficos
Autores principales: Usami, Shin-ichi, Nishio, Shin-ya, Nagano, Makoto, Abe, Satoko, Yamaguchi, Toshikazu
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2012
Materias:
Research Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3286470/
https://www.ncbi.nlm.nih.gov/pubmed/22384008
http://dx.doi.org/10.1371/journal.pone.0031276

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3286470/
https://www.ncbi.nlm.nih.gov/pubmed/22384008
http://dx.doi.org/10.1371/journal.pone.0031276

Ejemplares similares