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-Reference-Cited by-同舟云学术

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

Published:2006-02 Issue:2 Volume:340 Page:583-588
ISSN:0006-291X
Container-title:Biochemical and Biophysical Research Communications
language:en
Short-container-title:Biochemical and Biophysical Research Communications

Author:

Wang Qiuju,Li Qing-Zhong,Han Dongyi,Zhao Yali,Zhao Lidong,Qian Yaping,Yuan Hu,Li Ronghua,Zhai Suoqiang,Young Wie-Yen,Guan Min-Xin

Publisher

Elsevier BV

Subject

Cell Biology,Molecular Biology,Biochemistry,Biophysics

Reference34 articles.

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2. Molecular pathogenetic mechanism of maternally inherited deafness;Guan;Ann. N. Y. Acad. Sci.,2004

3. Susceptibility mutations in the mitochondrial small ribosomal RNA gene in aminoglycoside induced deafness;Bacino;Pharmacogenetics,1995

4. Inherited susceptibility to aminoglycoside ototoxicity: genetic heterogeneity and clinical implications;Casano;Am. J. Otolaryngol.,1999

5. Molecular analysis of mitochondrial 12S rRNA and tRNASer(UCN) genes in pediatric subjects with nonsyndromic hearing loss;Li;J. Med. Genet.,2004

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