Zebrafish Ciliopathy Screen Plus Human Mutational Analysis Identifies C21orf59 and CCDC65 Defects as Causing Primary Ciliary Dyskinesia
Title:
Zebrafish Ciliopathy Screen Plus Human Mutational Analysis Identifies C21orf59 and CCDC65 Defects as Causing Primary Ciliary Dyskinesia
Author:
Austin-Tse, Christina Halbritter, Jan Zariwala, Maimoona A. Gilberti, Renée M. Gee, Heon Yung Hellman, Nathan Pathak, Narendra Liu, Yan Panizzi, Jennifer R. Patel-King, Ramila S. Tritschler, Douglas Bower, Raqual O’Toole, Eileen Porath, Jonathan D. Hurd, Toby W. Chaki, Moumita Diaz, Katrina A. Kohl, Stefan Lovric, Svjetlana Hwang, Daw-Yang Braun, Daniela A. Schueler, Markus Airik, Rannar Otto, Edgar A. Leigh, Margaret W. Noone, Peadar G. Carson, Johnny L. Davis, Stephanie D. Pittman, Jessica E. Ferkol, Thomas W. Atkinson, Jeffry J. Olivier, Kenneth N. Sagel, Scott D. Dell, Sharon D. Rosenfeld, Margaret Milla, Carlos E. Loges, Niki T. Omran, Heymut Porter, Mary E. King, Stephen M. Knowles, Michael R. Drummond, Iain A. Hildebrandt, Friedhelm