Prevalence and Clinical Features of Hearing Loss Patients with CDH23 Mutations: A Large Cohort Study

Screening for gene mutations in CDH23, which has many exons, has lagged even though it is likely to be an important cause for hearing loss patients. To assess the importance of CDH23 mutations in non-syndromic hearing loss, two-step screening was applied and clinical characteristics of the patients...

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Detalles Bibliográficos
Autores principales: Miyagawa, Maiko, Nishio, Shin-ya, Usami, Shin-ichi
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/PMC3416829/
https://www.ncbi.nlm.nih.gov/pubmed/22899989
http://dx.doi.org/10.1371/journal.pone.0040366

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3416829/
https://www.ncbi.nlm.nih.gov/pubmed/22899989
http://dx.doi.org/10.1371/journal.pone.0040366

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