Fifteen-year follow-up of pulmonary function in individuals heterozygous for the cystic fibrosis phenylalanine-508 deletion
Research output: Contribution to journal › Journal article › Research › peer-review
In a cross-sectional study, we previously showed that cystic fibrosis phenylalanine-508 deletion (DeltaF508) heterozygosity may be overrepresented among individuals with asthma.
|Journal||Journal of Allergy and Clinical Immunology|
|Number of pages||6|
|Publication status||Published - May 2001|
- Adult, Aged, Asthma, Codon, Cystic Fibrosis, Cystic Fibrosis Transmembrane Conductance Regulator, DNA Mutational Analysis, Denmark, Female, Follow-Up Studies, Forced Expiratory Volume, Gene Frequency, Genetic Predisposition to Disease, Heterozygote, Humans, Lung Diseases, Obstructive, Male, Middle Aged, Odds Ratio, Polymerase Chain Reaction, Respiratory Function Tests, Risk Factors, Sequence Deletion, Smoking, Vital Capacity