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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. [electronic resource] by
- Ben Said, Mariem
- Grati, M'hamed
- Ishimoto, Takahiro
- Zou, Bing
- Chakchouk, Imen
- Ma, Qi
- Yao, Qi
- Hammami, Bouthaina
- Yan, Denise
- Mittal, Rahul
- Nakamichi, Noritaka
- Ghorbel, Abdelmonem
- Neng, Lingling
- Tekin, Mustafa
- Shi, Xiao Rui
- Kato, Yukio
- Masmoudi, Saber
- Lu, Zhongmin
- Hmani, Mounira
- Liu, Xuezhong
Producer: 20160831
In:
Human genetics vol. 135
Availability: No items available.
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