Literature DB >> 10080176

Deafness linked to DFNA2: one locus but how many genes?

P Van Hauwe, P J Coucke, F Declau, H Kunst, R J Ensink, H A Marres, C W Cremers, B Djelantik, S D Smith, P Kelley, P H Van de Heyning, G Van Camp.   

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Year:  1999        PMID： 10080176     DOI： 10.1038/6778

Source DB:  PubMed          Journal:  Nat Genet        ISSN： 1061-4036            Impact factor:   38.330


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  2 in total

1.  Clue to a new deafness gene: a large Chinese nonsyndromic hearing loss family linked to DFNA4.

Authors:  Liang Zong; Chunye Lu; Yali Zhao; Qian Li; Dongyi Han; Weiyan Yang; Yan Shen; Qingyin Zheng; Qiuju Wang
Journal:  J Genet Genomics       Date:  2012-11-16       Impact factor: 4.275

2.  Digenic inheritance of non-syndromic deafness caused by mutations at the gap junction proteins Cx26 and Cx31.

Authors:  Xue-Zhong Liu; Yongyi Yuan; Denise Yan; Emilie Hong Ding; Xiao Mei Ouyang; Yu Fei; Wenxue Tang; Huijun Yuan; Qing Chang; Li Lin Du; Xin Zhang; Guojian Wang; Shoeb Ahmad; Dong Yang Kang; Xi Lin; Pu Dai
Journal:  Hum Genet       Date:  2008-12-03       Impact factor: 4.132
  2 in total

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