ArticleAmerican journal of human genetics1999
Heterogenous point mutations in the mitochondrial tRNA Ser(UCN) precursor coexisting with the A1555G mutation in deaf students from Mongolia.
Article in American journal of human genetics, 1999. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 22 papers, 1 of them a synthesis that pooled it.
What it found
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The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.
The trial behind it
Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.
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Who cites it
22 citing papers in PubMed, 1 synthesis or guideline pooled it, 84 citations in OpenAlex.
- Genetics Evaluation Guidelines for the Etiologic Diagnosis of Congenital Hearing Loss. Genetic Evaluation of Congenital Hearing Loss Expert Panel. ACMG statement.Genetics in medicine : official journal of the American College of Medical GeneticsGuideline
- Frequency of mitochondrial mutations in non-syndromic hearing loss as well as possibly responsible variants found by whole mitochondrial genome screening.Journal of human genetics · 2014Trial
- Systematic genetic assessment of hearing loss using whole-genome sequencing identifies pathogenic variants.Experimental & molecular medicine · 2025Article
- Prevalence and Clinical Characteristics of Mitochondrial DNA Mutations in Korean Patients With Sensorineural Hearing Loss.Journal of Korean medical science · 2023Article
- The Mitochondrial tRNALife (Basel, Switzerland) · 2023Review
- Review
- Screening of deafness-causing DNA variants that are common in patients of European ancestry using a microarray-based approach.PloS one · 2017Article
- Genetics of non syndromic hearing loss.Medical journal, Armed Forces India · 2015Review
- Complex IV subunit 1 defect predicts postoperative survival in hepatocellular carcinoma.Oncology letters · 2014Article
- Compound mitochondrial DNA mutations in a neurological patient with ataxia, myoclonus and deafness.Journal of genetics · 2014Article
- Mitochondrial DNA mutation screening in an ethnically diverse nonsyndromic deafness cohort.Genetic testing and molecular biomarkers · 2012Article
- Absence of GJB2 gene mutations, the GJB6 deletion (GJB6-D13S1830) and four common mitochondrial mutations in nonsyndromic genetic hearing loss in a South African population.International journal of pediatric otorhinolaryngology · 2011Article
- GJB2 mutations in Mongolia: complex alleles, low frequency, and reduced fitness of the deaf.Annals of human genetics · 2010Article
- The genetic bases for non-syndromic hearing loss among Chinese.Journal of human genetics · 2009Review
- Audiological and genetic features of the mtDNA mutations.Acta oto-laryngologica · 2008Article
- GJB2 and mitochondrial A1555G gene mutations in nonsyndromic profound hearing loss and carrier frequencies in healthy individuals.Journal of genetics · 2008Article
- The ND4 G11696A mutation may influence the phenotypic manifestation of the deafness-associated 12S rRNA A1555G mutation in a four-generation Chinese family.Biochemical and biophysical research communications · 2007Article
- Cosegregation of the G7444A mutation in the mitochondrial COI/tRNA(Ser(UCN)) genes with the 12S rRNA A1555G mutation in a Chinese family with aminoglycoside-induced and nonsyndromic hearing loss.American journal of medical genetics. Part A · 2005Article
- Origins and frequencies of SLC26A4 (PDS) mutations in east and south Asians: global implications for the epidemiology of deafness.Journal of medical genetics · 2003Article
- Frequency of mtDNA A1555G and A7445G mutations among children with prelingual deafness in Turkey.European journal of pediatrics · 2003Article
Corrections and comments
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Authors and funding
9 authors at 2 institutions in 2 countries.
Funding
Abstract
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Registered trials
Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.