The most important problem for cystic fibrosis (CF) patients is the airway infections responsible for the gradually decreasing lung function as the infections persist. We have investigated properties that may be involved in persistence of P. aeruginosa (PA) in the lungs of young CF children by combining genomics, “phenomics” (phenotypes and molecular data), and clinical data.
|Publication status||Published - 2015|
|Event||The 29th Annual North American Cystic Fibrosis Conference - Phoenix, United States|
Duration: 8 Oct 2015 → 10 Oct 2015
Conference number: 29
|Conference||The 29th Annual North American Cystic Fibrosis Conference|
|Period||08/10/2015 → 10/10/2015|