Expression of the cystic fibrosis transmembrane conductance regulator gene in the respiratory tract of normal individuals and individuals with cystic fibrosis.

The most common mutation of the cystic fibrosis transmembrane conductance regulator gene, CFTR, associated with the clinical disorder cystic fibrosis (CF) is called "delta Phe508," a triple-base deletion resulting in loss of phenylalanine at residue 508 of the predicted 1480-amino acid CFT...

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Bibliografiska uppgifter
Huvudupphovsmän: Trapnell, B C, Chu, C S, Paakko, P K, Banks, T C, Yoshimura, K, Ferrans, V J, Chernick, M S, Crystal, R G
Materialtyp: Artigo
Språk:Inglês
Publicerad: 1991
Ämnen:
Research Article
Länkar:https://ncbi.nlm.nih.gov/pmc/articles/PMC52127/
https://ncbi.nlm.nih.gov/pubmed/1713683
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