Functional Mutation of SMAC/DIABLO, Encoding a Mitochondrial Proapoptotic Protein, Causes Human Progressive Hearing Loss DFNA64

Author:

Cheng Jing,Zhu Yuhua,He Sudan,Lu Yanping,Chen Jing,Han Bing,Petrillo Marco,Wrzeszczynski Kazimierz O.,Yang Shiming,Dai Pu,Zhai Suoqiang,Han Dongyi,Zhang Michael Q.,Li Wei,Liu Xuezhong,Li Huawei,Chen Zheng-Yi,Yuan Huijun

Publisher

Elsevier BV

Subject

Genetics(clinical),Genetics

Reference24 articles.

1. Ageing and hearing loss;Liu;J. Pathol.,2007

2. Hearing loss: Mechanisms revealed by genetics and cell biology;Dror;Annu. Rev. Genet.,2009

3. [Prevalence and etiology of people with hearing impairment in China];Sun;Zhonghua Liu Xing Bing Xue Za Zhi,2008

4. Non-syndromic autosomal-dominant deafness;Petersen;Clin. Genet.,2002

5. At the speed of sound: gene discovery in the auditory system;Resendes;Am. J. Hum. Genet.,2001

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