mtDNA mutation C1494T, haplogroup A, and hearing loss in Chinese
Author:
Publisher
Elsevier BV
Subject
Cell Biology,Molecular Biology,Biochemistry,Biophysics
Reference25 articles.
1. Mitochondrial ribosomal RNA mutation associated with both antibiotic-induced and non-syndromic deafness;Prezant;Nat. Genet.,1993
2. Mitochondrial dysfunction in hearing loss;Fischel-Ghodsian;Mitochondrion,2004
3. Genetic factors in aminoglycoside toxicity;Fischel-Ghodsian;Pharmacogenomics,2005
4. Functional characterization of the mitochondrial 12S rRNA C1494T mutation associated with aminoglycoside-induced and non-syndromic hearing loss;Zhao;Nucleic Acids Res.,2005
5. Maternally inherited aminoglycoside-induced and nonsyndromic deafness is associated with the novel C1494T mutation in the mitochondrial 12S rRNA gene in a large Chinese family;Zhao;Am. J. Hum. Genet.,2004
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2. Investigation of the mtDNA mutations in Syrian families with non-syndromic sensorineural hearing loss;International Journal of Pediatric Otorhinolaryngology;2018-10
3. Analysis of mitochondrial alterations in Brazilian patients with sensorineural hearing loss using MALDI-TOF mass spectrometry;BMC Medical Genetics;2016-05-26
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