A Rapid Method for Simultaneous Screening of Multi-Gene Mutations Associated with Hearing Loss in the Korean Population

Hearing loss (HL) is a congenital disease with a high prevalence, and patients with hearing loss need early diagnosis for treatment and prevention. The GJB2, MT-RNR1, and SLC26A4 genes have been reported as common causative genes of hearing loss in the Korean population and some mutations of these g...

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Detalles Bibliográficos
Autores principales: Sagong, Borum, Baek, Jeong-In, Oh, Se-Kyung, Na, Kyung Jin, Bae, Jae Woong, Choi, Soo Young, Jeong, Ji Yun, Choi, Jae Young, Lee, Sang-Heun, Lee, Kyu-Yup, Kim, Un-Kyung
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2013
Materias:
Research Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3585873/
https://www.ncbi.nlm.nih.gov/pubmed/23469187
http://dx.doi.org/10.1371/journal.pone.0057237

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3585873/
https://www.ncbi.nlm.nih.gov/pubmed/23469187
http://dx.doi.org/10.1371/journal.pone.0057237

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