Search Results - Deafness Gene Study Consortium

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    The prevalence and clinical features of MYO7A-related hearing loss including DFNA11, DFNB2 and USH1B by Kizuki Watanabe, Shin-ya Nishio, Shin-ichi Usami, the Deafness Gene Study Consortium

    Published in Scientific Reports (2024-04-01)
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    Simultaneous screening of multiple mutations by invader assay improves molecular diagnosis of hereditary hearing loss: a multicenter study. by Shin-ichi Usami, Shin-ya Nishio, Makoto Nagano, Satoko Abe, Toshikazu Yamaguchi, Deafness Gene Study Consortium

    Published in PLoS ONE (2012-01-01)
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