Neurootological findings of autosomal dominant non-syndromic deafness caused by a mutation in the myosin VIIBA gene

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作者
Kitamura, K [1 ]
Tamagawa, Y [1 ]
Kakoi, H [1 ]
机构
[1] Jichi Med Sch, Dept Otolaryngol, Tochigi, Japan
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Q189 [神经科学];
学科分类号
071006 ;
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页码:674 / 674
页数:1
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