Heterogeneity of phenotype in two cystic fibrosis patients homozygous for the CFTR exon 11 mutation G551D
about
Abdominal symptoms in cystic fibrosis and their relation to genotype, history, clinical and laboratory findings.Cystic fibrosis transmembrane conductance regulator is an epithelial cell receptor for clearance of Pseudomonas aeruginosa from the lung.Mechanosensitivity of wild-type and G551D cystic fibrosis transmembrane conductance regulator (CFTR) controls regulatory volume decrease in simple epithelia.Defective function of the cystic fibrosis-causing missense mutation G551D is recovered by genistein.
P2860
Heterogeneity of phenotype in two cystic fibrosis patients homozygous for the CFTR exon 11 mutation G551D
description
1996 nî lūn-bûn
@nan
1996 թուականի Օգոստոսին հրատարակուած գիտական յօդուած
@hyw
1996 թվականի օգոստոսին հրատարակված գիտական հոդված
@hy
1996年の論文
@ja
1996年論文
@yue
1996年論文
@zh-hant
1996年論文
@zh-hk
1996年論文
@zh-mo
1996年論文
@zh-tw
1996年论文
@wuu
name
Heterogeneity of phenotype in ...... he CFTR exon 11 mutation G551D
@ast
Heterogeneity of phenotype in ...... he CFTR exon 11 mutation G551D
@en
type
label
Heterogeneity of phenotype in ...... he CFTR exon 11 mutation G551D
@ast
Heterogeneity of phenotype in ...... he CFTR exon 11 mutation G551D
@en
prefLabel
Heterogeneity of phenotype in ...... he CFTR exon 11 mutation G551D
@ast
Heterogeneity of phenotype in ...... he CFTR exon 11 mutation G551D
@en
P2860
P356
P1476
Heterogeneity of phenotype in ...... he CFTR exon 11 mutation G551D
@en
P2093
P2860
P304
P356
10.1136/JMG.33.8.711
P407
P577
1996-08-01T00:00:00Z