The inner junction protein CFAP20 functions in motile and non-motile cilia and is critical for vision
Paul Chrystal(University of Toronto), Michel R. Leroux(Simon Fraser University)
Cited by 32
Related Papers
The centrosomal protein nephrocystin-6 is mutated in Joubert syndrome and activates transcription factor ATF4
|Nature Genetics|2006|573
Defects in the IFT-B Component IFT172 Cause Jeune and Mainzer-Saldino Syndromes in Humans
|The American Journal of Human Genetics|2013|232
TMEM231, mutated in orofaciodigital and Meckel syndromes, organizes the ciliary transition zone
|The Journal of Cell Biology|2015|108