Zebrafish Ciliopathy Screen Plus Human Mutational Analysis Identifies C21orf59 and CCDC65 Defects as Causing Primary Ciliary Dyskinesia
斑马鱼纤毛病筛查及人类突变分析确定 C21orf59 和 CCDC65 缺陷是导致原发性纤毛运动障碍的原因
期刊:American Journal of Human Genetics
影响因子:8.1
doi:10.1016/j.ajhg.2013.08.015
Christina Austin-Tse, Jan Halbritter, Maimoona A Zariwala, Renée M Gilberti, Heon Yung Gee, Nathan Hellman, Narendra Pathak, Yan Liu, Jennifer R Panizzi, Ramila S Patel-King, Douglas Tritschler, Raqual Bower, Eileen O'Toole, Jonathan D Porath, Toby W Hurd, Moumita Chaki, Katrina A Diaz, Stefan Kohl,