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A mutation in SLC22A4 encoding an organic cation transporter expressed in the cochlea strial endothelium causes human recessive non-syndromic hearing loss DFNB60 期刊论文
Human Genetics, 2016, 卷号: 135, 期号: 5, 页码: 513-524
作者:  Ben Said, Mariem;  Grati, M'hamed;  Ishimoto, Takahiro;  Zou, Bing;  Chakchouk, Imen
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