Systematic Analysis ofCCNOVariants in a Defined Population: Implications for Clinical Phenotype and Differential Diagnosis

Cyclin O (Ccno) functions during deuterosome-mediated centriole amplification of multiciliated cells

(2015) M. C. Funk et al.   EMBO JOURNAL

Unexpected genetic heterogeneity for primary ciliary dyskinesia in the Irish Traveller population

(2014) Jillian P Casey et al.   EUROPEAN JOURNAL OF HUMAN GENETICS

Nasal nitric oxide screening for primary ciliary dyskinesia: systematic review and meta-analysis

(2014) Samuel A. Collins et al.   EUROPEAN RESPIRATORY JOURNAL

Mutations in CCNO result in congenital mucociliary clearance disorder with reduced generation of multiple motile cilia

(2014) Julia Wallmeier et al.   NATURE GENETICS

MCIDAS mutations result in a mucociliary clearance disorder with reduced generation of multiple motile cilia

(2014) Mieke Boon et al.   Nature Communications

Mucociliary clearance: pathophysiological aspects

(2013) Mathias Munkholm et al.   CLINICAL PHYSIOLOGY AND FUNCTIONAL IMAGING

DYX1C1 is required for axonemal dynein assembly and ciliary motility

(2013) Aarti Tarkar et al.   NATURE GENETICS

Multicilin promotes centriole assembly and ciliogenesis during multiciliate cell differentiation

(2012) J. L. Stubbs et al.   NATURE CELL BIOLOGY

Factors influencing age at diagnosis of primary ciliary dyskinesia in European children

(2010) C. E. Kuehni et al.   EUROPEAN RESPIRATORY JOURNAL

Mutations in DNAH5 account for only 15% of a non-preselected cohort of patients with primary ciliary dyskinesia

(2009) M Failly et al.   JOURNAL OF MEDICAL GENETICS