Wordt geladen...

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...

Volledige beschrijving

Bewaard in:
Bibliografische gegevens
Hoofdauteurs: Trapnell, B C, Chu, C S, Paakko, P K, Banks, T C, Yoshimura, K, Ferrans, V J, Chernick, M S, Crystal, R G
Formaat: Artigo
Taal:Inglês
Gepubliceerd in: 1991
Onderwerpen:
Online toegang:https://ncbi.nlm.nih.gov/pmc/articles/PMC52127/
https://ncbi.nlm.nih.gov/pubmed/1713683
Tags: Voeg label toe
Geen labels, Wees de eerste die dit record labelt!