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Increased prevalence of mutations in the cystic fibrosis transmembrane conductance regulator in children with chronic rhinosinusitis

✍ Scribed by Raman, Vidya; Clary, Randall; Siegrist, Karen; Zehnbauer, Barbara; Chatila, Talal

Book ID
119490217
Publisher
Elsevier Science
Year
2002
Tongue
English
Weight
132 KB
Volume
109
Category
Article
ISSN
1097-6825

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Three mutations in the cystic fibrosis transmembrane conductance regulator (CFTR) gene were discovered in a pancreas-insufficient patient with cystic fibrosis (CF) who displayed an uncommon combination of almost normal chloride concentration in sweat tests and typical symptoms of gastrointestinal an