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Article

Mitochondrial DNA mutation screening in an ethnically diverse nonsyndromic deafness cohort.

Genetic testing and molecular biomarkers - 1 Sept 2012

Vivero Richard J, Ouyang Xiaomei, Yan Denise, Du Lilin, Liu Wendy, Angeli Simon I, Liu Xue Zhong

Abstract excerpt

Deafness is a heterogeneous trait with many known genetic and environmental causes. Hereditary hearing loss is an extremely common disorder in the general population. Mutations in mitochondrial DNA (mtDNA) are known to be associated with nonsyndromic deafness (NSD) and syndromic deafness. The objective of this article is to investigate the frequency of common mitochondrial mutations (A1555G, G7444A, and A3243G)...

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Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

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Share to Polymorphism, Restriction Fragment Length

Source

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Identifiers

PMID: 22853457
DOI: 10.1089/gtmb.2011.0365
PMCID: PMC3438807

Provenance

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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