IFT88 mutations identified in individuals with non-syndromic recessive retinal degeneration result in abnormal ciliogenesis
在患有非综合征性隐性视网膜变性的个体中发现的 IFT88 突变导致纤毛发生异常
期刊:Human Genetics
影响因子:3.8
doi:10.1007/s00439-018-1897-9
Anil Chekuri, Aditya A Guru, Pooja Biswas, Kari Branham, Shyamanga Borooah, Angel Soto-Hermida, Michael Hicks, Naheed W Khan, Hiroko Matsui, Akhila Alapati, Pongali B Raghavendra, Susanne Roosing, Sripriya Sarangapani, Sinnakaruppan Mathavan, Amalio Telenti, John R Heckenlively, S Amer Riazuddin, Ke