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; et al. (Human Genetics, 2016)

Polymorphisms in the XPG gene and risk of gastric cancer in Chinese populations - Jing He; Li-Xin Qiu; Meng-Yun Wang; Rui-Xi Hua; Ruo-Xin Zhang; Hong-Ping Yu; Ya-Nong Wang; Meng-Hong Sun; Xiao-Yan Zhou; Ya-Jun Yang; Jiu-Cun Wang; Li Jin; et al. (Human Genetics, 2012)