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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...

詳細記述

保存先:
書誌詳細
主要な著者: Trapnell, B C, Chu, C S, Paakko, P K, Banks, T C, Yoshimura, K, Ferrans, V J, Chernick, M S, Crystal, R G
フォーマット: Artigo
言語:Inglês
出版事項: 1991
主題:
オンライン・アクセス:https://ncbi.nlm.nih.gov/pmc/articles/PMC52127/
https://ncbi.nlm.nih.gov/pubmed/1713683
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