Extremely low penetrance of deafness associated with the mitochondrial 12S rRNA T1095C mutation in three Chinese families-Reference-Cited by-同舟云学术

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Extremely low penetrance of deafness associated with the mitochondrial 12S rRNA T1095C mutation in three Chinese families

Published:2006-09 Issue:1 Volume:348 Page:200-205
ISSN:0006-291X
Container-title:Biochemical and Biophysical Research Communications
language:en
Short-container-title:Biochemical and Biophysical Research Communications

Author:

Dai Pu,Yuan Yongyi,Huang Deliang,Qian Yaping,Liu Xin,Han Dongyi,Yuan Huijun,Wang Xinjiang,Young Wie-Yen,Guan Min-Xin

Publisher

Elsevier BV

Subject

Cell Biology,Molecular Biology,Biochemistry,Biophysics

Reference31 articles.

1. Prevalence of mitochondrial 12S rRNA mutations associated with aminoglycoside ototoxicity;Guan;The Volta Review,2005

2. Genetic factors in aminoglycoside toxicity;Fischel-Ghodsian;Pharmacogenomics,2005

3. 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

4. Functional characterization of the mitochondrial 12S rRNA C1494T mutation associated with aminoglycoside-induced and nonsyndromic hearing loss;Zhao;Nucleic Acid Res.,2005

5. Clinical and molecular analysis of a four-generation Chinese family with aminoglycoside-induced and nonsyndromic hearing loss associated with the mitochondrial 12S rRNA C1494T mutation;Wang;Biochem. Biophys. Res. Commun.,2006

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1. Increased risk of hearing loss associated with MT-RNR1 gene mutations: a real-world investigation among Han Taiwanese Population;BMC Medical Genomics;2024-06-05

2. Pharmacogénétique de l’ototoxicité des aminosides : état des connaissances et des pratiques – recommandations du Réseau francophone de pharmacogénétique (RNPGx);Therapies;2024-06

3. Pharmacogenomics and adverse effects of anti‐infective drugs in children;Clinical and Experimental Pharmacology and Physiology;2023-10-15

4. Novel mitochondrial gene variants in Northwestern Chinese probands with non-syndromic hearing loss by whole mitochondrial genome screening;Gene;2018-04

5. Audiological Follow-Up of Children with the m.1555A>G Mutation in Mitochondrial DNA;Audiology and Neurotology;2013

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