Identification of a novel homozygous nonsense mutation in EYS in a Chinese family with autosomal recessive retinitis pigmentosa by Huang Yukan, Zhang Jing, Li Chang, Yang Guohua, Liu Mugen, Wang Qing K, Tang Zhaohui

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Identification of a novel <it>KCNQ1 </it>mutation associated with both Jervell and Lange-Nielsen and Romano-Ward forms of long QT syndrome in a Chinese family by Liu Jing, Yang Junguo, Cheng Lingling, Zhang Shirong, Wang Pengyun, Ren Xiang, Yin Ke, Zhang Su, Liu Mugen, Wang Qing

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A novel <it>DSPP </it>mutation is associated with type II dentinogenesis Imperfecta in a chinese family by Xu Chengqi, Wang Xiaotao, Chang Wei, Zhao Zhen, Qu Erjun, Chen Lanying, Liu Jingyu, Zhang Xianqin, Wang Qing K, Liu Mugen

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Protective effect of <it>KCNH2 </it>single nucleotide polymorphism K897T in LQTS families and identification of novel <it>KCNQ1 </it>and <it>KCNH2 </it>mutations by Oberti Carlos, Redfearn Sharon, Bryant Randall M, Liu Mugen, Zhang Li, Chen Shenghan, Zhang Xianqin, Vincent G Michael, Wang Qing K

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