ArticleEuropean journal of pediatrics2003
Frequency of mtDNA A1555G and A7445G mutations among children with prelingual deafness in Turkey.
Article in European journal of pediatrics, 2003. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers.
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Who cites it
14 citing papers in PubMed, 65 citations in OpenAlex.
- Mutation Analysis of the Common Deafness Genes in Patients with Nonsyndromic Hearing Loss in Linyi by SNPscan Assay.BioMed research international · 2016Trial
- Novel m.4268T>C mutation in the mitochondrial tRNAWorld journal of clinical cases · 2022Article
- A study of deafness-related genetic mutations as a basis for strategies to prevent hereditary hearing loss in Hebei, China.Intractable & rare diseases research · 2015Article
- Mutation Spectrum of Common Deafness-Causing Genes in Patients with Non-Syndromic Deafness in the Xiamen Area, China.PloS one · 2015Article
- Screening for the mitochondrial A1555G mutation among Egyptian patients with non-syndromic, sensorineural hearing loss.International journal of molecular epidemiology and genetics · 2014Article
- A truncating mutation in SERPINB6 is associated with autosomal-recessive nonsyndromic sensorineural hearing loss.American journal of human genetics · 2010Article
- Comprehensive molecular etiology analysis of nonsyndromic hearing impairment from typical areas in China.Journal of translational medicine · 2009Article
- The genetic bases for non-syndromic hearing loss among Chinese.Journal of human genetics · 2009Review
- GJB2 and mitochondrial A1555G gene mutations in nonsyndromic profound hearing loss and carrier frequencies in healthy individuals.Journal of genetics · 2008Article
- MRPS18CP2 alleles and DEFA3 absence as putative chromosome 8p23.1 modifiers of hearing loss due to mtDNA mutation A1555G in the 12S rRNA gene.BMC medical genetics · 2007Article
- Mutational analysis of the mitochondrial 12S rRNA gene in Chinese pediatric subjects with aminoglycoside-induced and non-syndromic hearing loss.Human genetics · 2005Article
- Review
- Prevalence of the mitochondrial DNA A1555G mutation in sensorineural deafness patients in island Southeast Asia.Journal of human genetics · 2003Article
- Screening of the mitochondrial A1555G mutation in patients with sensorineural hearing loss.Brazilian journal of otorhinolaryngologyArticle
Corrections and comments
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Authors and funding
9 authors at 3 institutions in 1 country.
Funding
No grant is acknowledged in the PubMed record.
Abstract
unlabelledConsiderable differences on the frequencies of the mitochondrial 12S rRNA A1555G and tRNA(Ser(UCN)) A7445G mutations have been reported in different populations. Our screening of 168 patients coming from independent Turkish families with prelingual sensorineural non-syndromic deafness revealed three deaf children with A1555G (1.8%) but no examples of A7445G. One proband with the mitochondrial A1555G mutation has also evidence for right parietal infarct on a brain imaging study, for which common thrombotic mutations were found to be negative.
conclusionThis study shows that the mitochondrial A1555G mutation is among the significant causes of prelingual non-syndromic deafness in the Turkish population.
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