Clinical phenotype of cystic fibrosis patients with the G551D mutation
Author:
Publisher
Oxford University Press (OUP)
Subject
General Medicine
Link
http://academic.oup.com/qjmed/article-pdf/102/11/793/4580162/hcp120.pdf
Reference20 articles.
1. Genotype and Phenotype in Cystic Fibrosis
2. Correlation between Genotype and Phenotype in Patients with Cystic Fibrosis
3. MODIFIER GENETICS: Cystic Fibrosis
4. GENOTYPE-PHENOTYPE RELATIONSHIPS IN CYSTIC FIBROSIS
5. Mechanism of G551D-CFTR (Cystic Fibrosis Transmembrane Conductance Regulator) Potentiation by a High Affinity ATP Analog
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1. Rate of Lung Function Decline in People with Cystic Fibrosis Having a Residual Function Gene Mutation;Pulmonary Therapy;2022-11-01
2. Long-term safety and efficacy of tezacaftor–ivacaftor in individuals with cystic fibrosis aged 12 years or older who are homozygous or heterozygous for Phe508del CFTR (EXTEND): an open-label extension study;The Lancet Respiratory Medicine;2021-02
3. The preclinical discovery and development of the combination of ivacaftor + tezacaftor used to treat cystic fibrosis;Expert Opinion on Drug Discovery;2020-04-15
4. Ivacaftor in cystic fibrosis with residual function: Lung function results from an N-of-1 study;Journal of Cystic Fibrosis;2020-01
5. Patient-reported outcomes in patients with cystic fibrosis with a G551D mutation on ivacaftor treatment: results from a cross-sectional study;BMC Pulmonary Medicine;2019-08-13
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