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Article

Audiological and genetic features of the mtDNA mutations.

Acta oto-laryngologica - 1 Jul 2008

Liu X Z, Angeli S, Ouyang X M, Liu W, Ke X M, Liu Y H, Liu S X, Du L L, Deng X W, Yuan H, Yan D

Abstract excerpt

CONCLUSIONS: Significant difference in the incidence of mitochondrial DNA (mtDNA) mutations was found between the Chinese and USA populations. The identification of the mtDNA A1555G mutation in a large proportion of Chinese probands with nonsyndromic sensorineural hearing loss (NSHL) provides a molecular explanation for the high prevalence of aminoglycoside-induced deafness in China. OBJECTIVE: The aim was to...

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Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

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Identifiers

PMID: 18568513
DOI: 10.1080/00016480701719011
PMCID: PMC4523053

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PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-07.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

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