Compound Heterozygosity of the Functionally Null Cdh23v-ngt and Hypomorphic Cdh23ahl/i Alleles Leads to Early-onset Progressive Hearing Loss in Mice
Compound Heterozygosity of the Functionally Null Cdh23v-ngt and Hypomorphic Cdh23ahl/i Alleles Leads to Early-onset Progressive Hearing Loss in Mice
复制标题
功能性无效 Cdh23v-ngt 和亚形 Cdh23ahl/i 等位基因的复合杂合性导致小鼠早发进行性听力损失
DOI：
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发表时间：
2013
期刊：
影响因子：
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通讯作者：
Kikkawa Y
中科院分区：
文献类型：
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作者：
Miyasaka Y;Suzuki S;Ohshiba Y;Watanabe K;Sagara Y;Yasuda SP;Matsuoka K;Shitara H;Yonekawa H;Kominami R;Kikkawa Y
