c.753_754delAG, a novel CFTR mutation found in a Chinese patient with cystic fibrosis: A case report and review of the literature
Frontiers | CFTR Modulators: The Changing Face of Cystic Fibrosis in the Era of Precision Medicine
Mutations of the cystic fibrosis transmembrane conductance regulator gene in males with congenital bilateral absence of the vas deferens: Reproductive implications and genetic counseling (Review)
Frequency of common CFTR gene mutations in Venezuelan patients with cystic fibrosis
mRNA‐based detection of rare CFTR mutations improves genetic diagnosis of cystic fibrosis in populations with high genetic heterogeneity - Felício - 2017 - Clinical Genetics - Wiley Online Library
IJMS | Free Full-Text | Combined Treatment of Bronchial Epithelial Calu-3 Cells with Peptide Nucleic Acids Targeting miR-145-5p and miR-101-3p: Synergistic Enhancement of the Expression of the Cystic Fibrosis Transmembrane Conductance Regulator (
Cystic Fibrosis and CFTR Gene
Genetics of cystic fibrosis: CFTR mutation classifications toward genotype-based CF therapies - ScienceDirect
Figure 1 from Identification of Unique Pattern of CFTR Gene Mutations in Cystic Fibrosis in an Ethnic Kashmiri Population (North India) | Semantic Scholar
Rapid identification of variants associated with cystic fibrosis using a long-read multiplexed amplicon panel
Helicase / Cystic Fibrosis
Mutations in the Cystic Fibrosis Gene in Patients with Congenital Absence of the Vas Deferens | NEJM
Cystic Fibrosis and CFTR Gene
Comparative genomic sequence analysis of the human and mouse cystic fibrosis transmembrane conductance regulator genes | PNAS
Schematic overview of the CFTR protein domains, with a close-up of the... | Download Scientific Diagram
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All-in-one NGS solution for cystic fibrosis diagnosis | BioVendor Group
Next-generation sequencing for identifying a novel/de novo pathogenic variant in a Mexican patient with cystic fibrosis: a case report | BMC Medical Genomics | Full Text
Cystic Fibrosis Mutation Database: CFTR Domains
Analysis of rearrangements of the CFTR gene in patients from Turkey with CFTR-related disorders: frequent exon 2 deletion | Journal of Human Genetics
Lecture 8-9 Preview
Accessory Protein Facilitated CFTR-CFTR Interaction, a Molecular Mechanism to Potentiate the Chloride Channel Activity: Cell
Genomic Sequence Analysis of Fugu rubripes CFTR and Flanking Genes in a 60 kb Region Conserving Synteny with 800 kb of Human Chromosome 7
DNA Sequence - Cystic Fibrosis & CFTR Gene
p.G970D is the most frequent CFTR mutation in Chinese patients with cystic fibrosis | Human Genome Variation
Synonymous mutations in CFTR exon 12 affect splicing and are not neutral in evolution | PNAS
