Discover Community Create You

Loading publication...

Noodle always counts identifier-free feature events for service operation. With your permission, Google Analytics can also estimate audience and engagement. Search text, publication identifiers, cookies, IP addresses and browser fingerprints are never included in Noodle's first-party event counters.

Privacy details

Article

Mutations in the two ribosomal RNA genes in mitochondrial DNA among Finnish children with hearing impairment.

BMC medical genetics - 4 Feb 2015

Häkli Sanna, Luotonen Mirja, Sorri Martti, Majamaa Kari

Abstract excerpt

BACKGROUND: Mutations in the two MT-RNR genes in mitochondrial DNA can cause hearing impairment that presents with variable severity and age of onset. In order to study the prevalence of mutations in MT-RNR1 and MT-RNR2 genes among Finnish children, we studied a ten-year cohort of hearing impaire...

Read the complete abstract on PubMed

Topics

Share this publication in a Topic to start or enrich a Post.

Share to Child
Share to Child, Preschool
Share to DNA, Mitochondrial

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Finland

Share to Genes, rRNA

Share to Haplotypes

Share to Hearing Loss

Share to Mutation

Source

Open in PubMed Open full text

Identifiers

PMID: 25650108
DOI: 10.1186/s12881-015-0145-6
PMCID: PMC4410458

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 4 Sept 2026. Prepared record publication-25650108-2026-09-04.2. Manifest publication-graph-cohort-2026-09-04.2.

Source receipt: PubMed via Helena Literature Corpus, retrieved 4 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Mutations in the two ribosomal RNA genes in mitochondrial DNA among Finnish children with hearing impairment.PMID 25650108Read ↗

Increased Risk of Hearing Loss Associated with MT-RNR1 Gene Mutations: A Real-World Investigation Among Han Taiwanese PopulationSemantic proximity Read ↗

Increased risk of hearing loss associated with MT-RNR1 gene mutations: a real-world investigation among Han Taiwanese Population.Semantic proximity Read ↗

Maternally inherited hearing impairment.Semantic proximity Read ↗

Genetic Epidemiology of Mitochondrial Pathogenic Variants Causing Nonsyndromic Hearing Loss in a Large Cohort of South Indian Hearing Impaired Individuals.Semantic proximity Read ↗

Mitochondrial tRNA mutations in 887 Chinese subjects with hearing loss.Semantic proximity Read ↗

Screening for mitochondrial 12S rRNA C1494T mutation in 655 patients with non-syndromic hearing loss: An observational study.Semantic proximity Read ↗

Mitochondrial mutations in maternally inherited hearing loss.Semantic proximity Read ↗

Prevalence and Clinical Characteristics of Mitochondrial DNA Mutations in Korean Patients With Sensorineural Hearing Loss.Semantic proximity Read ↗

Mitochondrial mutations in non-syndromic hearing loss at UAE.Semantic proximity Read ↗

Mitochondrial rRNA and tRNA and hearing function.Semantic proximity Read ↗

Whole mitochondrial genome screening in two families with hearing loss: detection of a novel mutation in the 12S rRNA gene.Semantic proximity Read ↗

Heteroplasmy for the 1555A>G mutation in the mitochondrial 12S rRNA gene in six Spanish families with non-syndromic hearing loss.Semantic proximity Read ↗

⌁Select a neighboring publication to make it the new centre.