Exome sequencing in a Chinese family reveals TTC9 mutation associated with keratitis-ichthyosis-deafness (KID) syndrome

作者：Xiaohua Wang, Xueli Wu, Baoqing Zheng, Yongfeng Chen, Daocheng Zheng · 发表于：European Journal of Dermatology · 年份：2018 · DOI：10.1684/ejd.2018.3330 · 被引用次数：2 · 研究领域：Cell Adhesion Molecules Research、Connexins and lens biology、RNA regulation and disease