Identification of a novel CDH23 gene variant associated with non-syndromic progressive hearing loss in a Chinese family: Individualized hearing rehabilitation guided by genetic diagnosis

Identification of a novel CDH23 gene variant associated with non-syndromic progressive hearing loss in a Chinese family: Individualized hearing rehabilitation guided by genetic diagnosis
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DOI：
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发表时间：
2019
期刊：
INT J PEDIATR OTORHI
影响因子：
1.5
通讯作者：
Wu H
Wu H
中科院分区：
医学4区
文献类型：
--
作者：
Chen Y;Li Y;Ren Y;Li HF;Huang MP;Jia H;Yang T;Wang ZY;Huang ZW;Wu H

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