Publication | Open Access

Association between genotype and pulmonary phenotype in cystic fibrosis patients with severe mutations

Mendelian DisorderGenetic DisorderGeneticsCystic Fibrosis PatientsGenetic EpidemiologyPathologyPulmonary FibrosisSevere MutationsPulmonary MedicinePulmonary PhenotypeDisease Gene IdentificationMedical GeneticsMedicineClinical Genetics