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Article

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

Brazilian journal of otorhinolaryngology - 1 Jan 2000

Jiang Hua, Chen Jia, Li Ying, Lin Peng-Fang, He Jian-Guo, Yang Bei-Bei

Abstract excerpt

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 study was to investigate the incidence of these mitochondrial DNA mutations in such population. METHODS: A total of...

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Topics

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Share to Child, Preschool
Share to DNA, Mitochondrial

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Hearing Loss, Sensorineural

Share to Infant

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Share to RNA, Ribosomal

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Source

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Identifiers

PMID: 26873147
DOI: 10.1016/j.bjorl.2015.06.006
PMCID: PMC9449052

Genes

GJB2
UCN

Provenance

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