Prevalence of mitochondrial DNA mutations in sporadic patients with nonsyndromic sensorineural hearing loss()

INTRODUCTION: Several mitochondrial DNA mutations have been reported to be associated with nonsyndromic hearing loss in several families. However, little is known about the prevalence of these mutations in sporadic patients with nonsyndromic sensorineural hearing loss. OBJECTIVE: The purpose of our...

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Detalles Bibliográficos
Autores principales: Jiang, Hua, Chen, Jia, Li, Ying, Lin, Peng-Fang, He, Jian-Guo, Yang, Bei-Bei
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2015
Materias:
Original Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9449052/
https://www.ncbi.nlm.nih.gov/pubmed/26873147
http://dx.doi.org/10.1016/j.bjorl.2015.06.006

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9449052/
https://www.ncbi.nlm.nih.gov/pubmed/26873147
http://dx.doi.org/10.1016/j.bjorl.2015.06.006

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