Disease-relevant mutations alter amino acid co-evolution networks in the second nucleotide binding domain of CFTR
Author:
Publisher
Public Library of Science (PLoS)
Subject
Multidisciplinary
Reference71 articles.
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3. The Relation between Genotype and Phenotype in Cystic Fibrosis—Analysis of the Most Common Mutation (ΔF508);E Kerem;N Engl J Med,1990
4. In vivo phosphorylation of CFTR promotes formation of a nucleotide-binding domain heterodimer;M Mense;EMBO J,2006
5. Thermodynamics of CFTR Channel Gating: A Spreading Conformational Change Initiates an Irreversible Gating Cycle;L Csanády;J Gen Physiol,2006
Cited by 3 articles. 订阅此论文施引文献 订阅此论文施引文献,注册后可以免费订阅5篇论文的施引文献,订阅后可以查看论文全部施引文献
1. Severity of the S1251N allele in cystic fibrosis is affected by the presence of the F508C variant in cis;Journal of Cystic Fibrosis;2022-07
2. Carrier frequency of CFTR variants in the non‐Caucasian populations by genome aggregation database (gnomAD)‐based analysis;Annals of Human Genetics;2020-06-02
3. Correction: Disease-relevant mutations alter amino acid co-evolution networks in the second nucleotide binding domain of CFTR;PLOS ONE;2020-02-27
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