Literature DB >> 10868221

Sensorineural hearing impairment non-syndromic, dominant DFNA11.

Y Tamagawa1, K Kitamura, T Ishida, M Nishizawa, X Z Liu, J Walsh, K P Steel, S D Brown.   

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Year:  2000        PMID： 10868221     DOI： 10.1159/000059092

Source DB:  PubMed          Journal:  Adv Otorhinolaryngol        ISSN： 0065-3071


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  3 in total

1.  A DNA variant within the MYO7A promoter regulates YY1 transcription factor binding and gene expression serving as a potential dominant DFNA11 auditory genetic modifier.

Authors:  Valerie A Street; Jin Li; Carol A Robbins; Jeremy C Kallman
Journal:  J Biol Chem       Date:  2011-03-04       Impact factor: 5.157

2.  In search of the DFNA11 myosin VIIA low- and mid-frequency auditory genetic modifier.

Authors:  Jeremy C Kallman; James O Phillips; Naomi F Bramhall; John P Kelly; Valerie A Street
Journal:  Otol Neurotol       Date:  2008-09       Impact factor: 2.311

3.  Identification and functional study of a new missense mutation in the motor head domain of myosin VIIA in a family with autosomal dominant hearing impairment (DFNA11).

Authors:  Qing Sang; Xukun Yan; Huan Wang; Ruizhi Feng; Xiang Fei; Duan Ma; Qinghe Xing; Qiaoli Li; Xinzhi Zhao; Li Jin; Lin He; Huawei Li; Lei Wang
Journal:  PLoS One       Date:  2013-01-29       Impact factor: 3.240
  3 in total

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