Cutting edge genetic studies in primary ciliary dyskinesia
- 1Cystic Fibrosis/Pulmonary Research and Treatment Center, University of North Carolina at Chapel Hill, Chapel Hill, North Carolina, USA
- 2Department of Pediatrics, University of North Carolina, Chapel Hill, North Carolina, USA
- 3Department of Pathology and Lab Medicine, University of North Carolina, Chapel Hill, North Carolina, USA
- Correspondence to Dr Michael R Knowles, Cystic Fibrosis/Pulmonary Research and Treatment Center, University of North Carolina at Chapel Hill, 7019 Thurston Bowles Building, CB# 7248, Chapel Hill 27599, North Carolina, USA; knowles{at}med.unc.edu
- Accepted 11 January 2012
- Published Online First 10 February 2012
- Airway epithelium
- atypical mycobacterial infection
- bacterial infection
- cystic fibrosis
- infection control
- nebuliser therapy
- rare lung diseases
- respiratory infection
- bronchiectasis
We would describe our genetic studies in primary ciliary dyskinesia1 as ‘cutting edge’, rather …
