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

被引：0
|
作者：
Kitamura, K [1 ]
Tamagawa, Y [1 ]
Kakoi, H [1 ]
机构：
[1] Jichi Med Sch, Dept Otolaryngol, Tochigi, Japan
来源：
EQUILIBRIUM RESEARCH, CLINICAL EQUILIBRIOMETRY AND MODERN TREATMENT | 2000年 / 1201卷
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中图分类号：
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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