Rapid identification of aminoglycoside-induced deafness gene mutations using multiplex real-time polymerase chain reaction-Reference-Cited by-同舟云学术

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Rapid identification of aminoglycoside-induced deafness gene mutations using multiplex real-time polymerase chain reaction

Published:2015-07 Issue:7 Volume:79 Page:1067-1072
ISSN:0165-5876
Container-title:International Journal of Pediatric Otorhinolaryngology
language:en
Short-container-title:International Journal of Pediatric Otorhinolaryngology

Author:

Huang Shasha,Xiang Guangxin,Kang Dongyang,Wang Chen,Kong Yanling,Zhang Xun,Liang Shujian,Mitchelson Keith,Xing Wanli,Dai Pu

Funder

Minister of Science and Technology of China

Chinese National Nature Science Foundation Research Grants

China Postdoctoral Science Foundation

Publisher

Elsevier BV

Subject

Otorhinolaryngology,General Medicine,Pediatrics, Perinatology and Child Health

Reference18 articles.

1. Nuclear background determines biochemical phenotype in the deafness-associated mitochondrial 12S rRNA mutation;Guan;Hum. Mol. Genet.,2001

2. The Second Main Data Bulletin of National Sample Survey on Disability. http://www.stats.gov.cn/tjsj/ndsj/shehui/2006/html/fu3.htm.

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. The aminoglycosides;Chamber,1996

5. Mitochondrial deafness;Kokotas;Clin. Genet.,2007

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