Diverse spectrum of rare deafness genes underlies early-childhood hearing loss in Japanese patients: a cross-sectional, multi-center next-generation sequencing study

BACKGROUND: Genetic tests for hereditary hearing loss inform clinical management of patients and can provide the first step in the development of therapeutics. However, comprehensive genetic tests for deafness genes by Sanger sequencing is extremely expensive and time-consuming. Next-generation sequ...

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Detalles Bibliográficos
Autores principales: Mutai, Hideki, Suzuki, Naohiro, Shimizu, Atsushi, Torii, Chiharu, Namba, Kazunori, Morimoto, Noriko, Kudoh, Jun, Kaga, Kimitaka, Kosaki, Kenjiro, Matsunaga, Tatsuo
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2013
Materias:
Research
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4231469/
https://www.ncbi.nlm.nih.gov/pubmed/24164807
http://dx.doi.org/10.1186/1750-1172-8-172

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4231469/
https://www.ncbi.nlm.nih.gov/pubmed/24164807
http://dx.doi.org/10.1186/1750-1172-8-172

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