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| Usher syndrome 1D and nonsyndromic autosomal recessive deafness DFNB12 are caused by allelic mutations of the novel cadherin-like gene CDH23 JM Bork, LM Peters, S Riazuddin, SL Bernstein, ZM Ahmed, SL Ness, ... The American Journal of Human Genetics 68 (1), 26-37, 2001 | 631 | 2001 |
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| Mutations in the γ-actin gene (ACTG1) are associated with dominant progressive deafness (DFNA20/26) M Zhu, T Yang, S Wei, AT DeWan, RJ Morell, JL Elfenbein, RA Fisher, ... The American Journal of Human Genetics 73 (5), 1082-1091, 2003 | 247 | 2003 |
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