High morbidity and mortality in cystic fibrosis patients compound heterozygous for 3905insT and ΔF508

European Respiratory Journal

Volumn 17, Issue 6, 2001, Pages 1181-1186

  Schibler, A ^a   Bolt, I ^a   Gallati, S ^a   Schoni M H ^a   Kraemer, R ^a  

^a UNIVERSITY CHILDREN S HOSPITAL   (Switzerland)

Author keywords

Conductance regulator gene; Cystic fibrosis transmembrane; Genotype phenotype association; Survival

Indexed keywords

CHLORIDE; TRANSMEMBRANE CONDUCTANCE REGULATOR;

ADOLESCENT; ADULT; AGE; ARTICLE; BACTERIAL COLONIZATION; CHILD; CLINICAL ARTICLE; CLINICAL FEATURE; COMPARATIVE STUDY; CONTROLLED STUDY; CYSTIC FIBROSIS; DEATH; DISEASE SEVERITY; FEMALE; FORCED EXPIRATORY VOLUME; GENE MUTATION; GENOTYPE; HETEROZYGOSITY; HOMOZYGOSITY; HUMAN; INFANT; LUNG DISEASE; LUNG FUNCTION; MALE; MORBIDITY; MORTALITY; ONSET AGE; PHENOTYPE; PREDICTION; PRIORITY JOURNAL; PSEUDOMONAS AERUGINOSA; SCORING SYSTEM; SURVIVAL RATE; SWEAT;

ADOLESCENT; ADULT; CHILD; CHILD, PRESCHOOL; CYSTIC FIBROSIS; CYSTIC FIBROSIS TRANSMEMBRANE CONDUCTANCE REGULATOR; FEMALE; FORCED EXPIRATORY VOLUME; GENOTYPE; HETEROZYGOTE DETECTION; HUMANS; INFANT; MALE; MUTATION; PHENOTYPE; PNEUMONIA, BACTERIAL; PSEUDOMONAS INFECTIONS; SURVIVAL ANALYSIS; VITAL CAPACITY;

EID: 0034888650     PISSN: 09031936     EISSN: None     Source Type: Journal    
DOI: 10.1183/09031936.01.00034601     Document Type: Article

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