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 CFTR protein....

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Detalhes bibliográficos

Publicado no:	Proc Natl Acad Sci U S A
Principais autores:	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 em:	National Academy of Sciences 1991
Assuntos:	Research Article
Acesso em linha:	https://ncbi.nlm.nih.govhttps://pmc.ncbi.nlm.nih.gov/articles/PMC52127/ https://ncbi.nlm.nih.govhttps://pubmed.ncbi.nlm.nih.gov/1713683/ https://ncbi.nlm.nih.govhttps://doi.org/10.1073/pnas.88.15.6565
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