Exome sequencing in a Chinese family reveals TTC9 mutation associated with keratitis-ichthyosis-deafness (KID) syndromeXiaohua Wang, Xueli Wu,Baoqing Zheng,Yongfeng Chen,Daocheng ZhengEuropean Journal of Dermatology(2018)引用 1|浏览3暂无评分AI 理解论文溯源树样例生成溯源树,研究论文发展脉络Chat Paper正在生成论文摘要