Extremely low penetrance of deafness associated with the mitochondrial 12S rRNA mutation in 16 Chinese families: Implication for early detection and prevention of deafness-Reference-Cited by-同舟云学术

Extremely low penetrance of deafness associated with the mitochondrial 12S rRNA mutation in 16 Chinese families: Implication for early detection and prevention of deafness

Published:2006-02 Issue:1 Volume:340 Page:194-199
ISSN:0006-291X
Container-title:Biochemical and Biophysical Research Communications
language:en
Short-container-title:Biochemical and Biophysical Research Communications

Author:

Dai Pu,Liu Xin,Han Dongyi,Qian Yaping,Huang Deliang,Yuan Huijun,Li Weiming,Yu Fei,Zhang Ruining,Lin Hongyan,He Yong,Yu Youjun,Sun Quanzhu,Qin Huaiyi,Li Ronghua,Zhang Xin,Kang Dongyang,Cao Juyang,Young Wie-Yen,Guan Min-Xin

Publisher

Elsevier BV

Subject

Cell Biology,Molecular Biology,Biochemistry,Biophysics

Reference30 articles.

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4. Unique inheritance of streptomycin-induced deafness;Higashi;Clin. Genet.,1989

5. Mutational analysis of the mitochondrial 12S rRNA gene in Chinese pediatric subjects with aminoglycoside induced and non-syndromic hearing loss;Li;Hum. Genet.,2005

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