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Detection of hyphomycetes in the upper respiratory tract of patients with cystic fibrosis

✍ Scribed by R. Horré; G. Marklein; R. Siekmeier; S.-M. Reiffert

Book ID
108916881
Publisher
John Wiley and Sons
Year
2010
Tongue
English
Weight
152 KB
Volume
54
Category
Article
ISSN
0933-7407

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Mutations in the human genome may result in altered phenotypes. The cystic fibrosis (CF) patient, for instance, suffers from an aberrant composition of the epithelial lining of the gastrointestinal and respiratory tract. In this particular case, a single point mutation in the cystic fibrosis conduct