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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Main Authors: Trapnell, B C, Chu, C S, Paakko, P K, Banks, T C, Yoshimura, K, Ferrans, V J, Chernick, M S, Crystal, R G
Formato: Artigo
Idioma:Inglês
Publicado: 1991
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Research Article
Acceso en liña:https://ncbi.nlm.nih.gov/pmc/articles/PMC52127/
https://ncbi.nlm.nih.gov/pubmed/1713683
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