Varaico: Literature-Extracted Genetic Variants

Gene:CFTR
Variant:p.R560Splc
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CFTR

NM_000492.4:p.R560Splc

Associated Papers

Elexacaftor-tezacaftor-ivacaftor in people with cystic fibrosis harbouring two CFTR Class I variants: real-world data from the French compassionate programme.

Burgel PR et al.

Eclinicalmedicine, 2025

40932846 (PubMed )
Supplement: mmc2.xlsx › EXCEPTIONAL

Identification and Characterization of a Rare Exon 22 Duplication in CFTR in Two Families.

Ahting S et al.

International Journal of Molecular Sciences, 2025

40429633 (PubMed )
Supplement: ijms-26-04487-s001.zip › CFTR2_25September2024.xlsx › CFTR2_variants__genomic_info

Study of the genetic and molecular epidemiology of cystic fibrosis based on the patient registry for planning targeted therapy in Russian Federation.

Kondratyeva E et al.

Frontiers in Genetics, 2024

39529847 (PubMed )
Supplement: Table1.XLSX › Supplement_1

A comprehensive review of cystic fibrosis in Africa and Asia.

Abubakar Bobbo K et al.

Saudi Journal of Biological Sciences, 2023

A review of cystic fibrosis: Basic and clinical aspects.

Chen Q et al.

Animal Models and Experimental Medicine, 2021

Whole-Exome Sequencing Identified CFTR Variants in Two Consanguineous Families in China.

Yang B et al.

Frontiers in Genetics, 2021

34276759 (PubMed )
Supplement: Data_Sheet_1.docx

A systematic review of the clinical and genetic characteristics of Chinese patients with cystic fibrosis.

Shi R et al.

Pediatric Pulmonology, 2020

Characterization of clinical and genetic spectrum of Chinese patients with cystic fibrosis.

Liu K et al.

Orphanet Journal of Rare Diseases, 2020

c.753_754delAG, a novel CFTR mutation found in a Chinese patient with cystic fibrosis: A case report and review of the literature.

Wang YQ et al.

World Journal of Clinical Cases, 2019

Liver Failure in a Chinese Cystic Fibrosis Child With Homozygous R553X Mutation.

Li H et al.

Frontiers in Pediatrics, 2019

Four case reports of Chinese cystic fibrosis patients and literature review.

Xu J et al.

Pediatric Pulmonology, 2017

Differences in gene mutations between Chinese and Caucasian cystic fibrosis patients.

Zheng B et al.

Pediatric Pulmonology, 2017

CFTR founder mutation causes protein trafficking defects in Chinese patients with cystic fibrosis.

Leung GK et al.

Molecular Genetics & Genomic Medicine, 2017

p.G970D is the most frequent CFTR mutation in Chinese patients with cystic fibrosis.

Tian X et al.

Human Genome Variation, 2016

Epidemiology and genetics of cystic fibrosis in Asia: In preparation for the next-generation treatments.

Singh M et al.

Respirology (carlton, Vic.), 2015

Characterization of gene mutations and phenotypes of cystic fibrosis in Chinese patients.

Liu Y et al.

Respirology (carlton, Vic.), 2015

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Regarding the variants extracted from papers and shown text snippets from research papers, the following holds: "Some rights reserved. This work permits non-commercial use, distribution and reproduction in any medium, provided the original author and source are credited."