A mutation in SLC22A4 encoding an organic cation transporter expressed in the cochlea strial endothelium causes human recessive non-syndromic hearing loss DFNB60

Mariem Ben Said, M’hamed Grati, Takahiro Ishimoto, Bing Zou, Imen Chakchouk, Qi Ma, Qi Yao, Bouthaina Hammami, Denise Yan, Rahul Mittal, Noritaka Nakamichi, Abdelmonem Ghorbel, Lingling Neng, Mustafa Tekin, Xiao Rui Shi, Yukio Kato, Saber Masmoudi, Zhongmin Lu, Mounira Hmani, Xuezhong Liu

Research output: Contribution to journal › Article › peer-review

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Medicine & Life Sciences