DeltaF508 heterozygosity in cystic fibrosis and susceptibility to asthma
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DeltaF508 heterozygosity in cystic fibrosis and susceptibility to asthma. / Dahl, Morten; Tybjaerg-Hansen, A; Lange, P; Nordestgaard, B G.
In: Lancet, Vol. 351, No. 9120, 27.06.1998, p. 1911-3.Research output: Contribution to journal › Journal article › Research › peer-review
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TY - JOUR
T1 - DeltaF508 heterozygosity in cystic fibrosis and susceptibility to asthma
AU - Dahl, Morten
AU - Tybjaerg-Hansen, A
AU - Lange, P
AU - Nordestgaard, B G
PY - 1998/6/27
Y1 - 1998/6/27
N2 - Cystic fibrosis is a recessive disorder mainly characterised by lung disease. We tested the hypothesis that individuals heterozygous for the common cystic fibrosis deltaF508 mutation are at risk of obstructive pulmonary disease.
AB - Cystic fibrosis is a recessive disorder mainly characterised by lung disease. We tested the hypothesis that individuals heterozygous for the common cystic fibrosis deltaF508 mutation are at risk of obstructive pulmonary disease.
KW - Asthma
KW - Cross-Sectional Studies
KW - Cystic Fibrosis
KW - Cystic Fibrosis Transmembrane Conductance Regulator
KW - Denmark
KW - Disease Susceptibility
KW - Female
KW - Heterozygote
KW - Heterozygote Detection
KW - Humans
KW - Male
KW - Middle Aged
KW - Spirometry
M3 - Journal article
C2 - 9654257
VL - 351
SP - 1911
EP - 1913
JO - The Lancet
JF - The Lancet
SN - 0140-6736
IS - 9120
ER -
ID: 45524424