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)

A novel variant in the 3′ UTR of human SCN1A gene from a patient with Dravet syndrome decreases mRNA stability mediated by GAPDH’s binding - Tao Zeng; Zhao-Fei Dong; Shu-Jing Liu; Rui-Ping Wan; Ling-Jia Tang; Ting Liu; Qi-Hua Zhao; Yi-Wu Shi; Yong-Hong Yi; Wei-Ping Liao; Yue-Sheng Long (Human Genetics, 2014)

A miR-570 binding site polymorphism in the B7-H1 gene is associated with the risk of gastric adenocarcinoma - Weipeng Wang; Fang Li; Yong Mao; Huan Zhou; Jing Sun; Rui Li; Cuiping Liu; Weichang Chen; Dong Hua; Xueguang Zhang (Human Genetics, 2013)