Zebrafish Ciliopathy Screen Plus Human Mutational Analysis Identifies C21orf59 and CCDC65 Defects as Causing Primary Ciliary DyskinesiaChristina Austin‐Tse, Friedhelm Hildebrandt, Jan Halbritter et al.|The American Journal of Human Genetics|2013Cited by 201
Mutation of Growth Arrest Specific 8 Reveals a Role in Motile Cilia Function and Human DiseaseWesley Lewis, Nicolas F. Berbari, Erik B. Malarkey et al.|PLoS Genetics|2016Cited by 43