A mutation in SLC22A4 encoding an organic cation transporter expressed in the cochlea strial endothelium causes human recessive non-syndromic hearing loss DFNB60
编码耳蜗纹内皮中表达的有机阳离子转运蛋白的 SLC22A4 突变导致人类隐性非综合征性听力损失 DFNB60
期刊:Human Genetics
影响因子:3.8
doi:10.1007/s00439-016-1657-7
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 Liu1