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Article

Influence of the duplication of CFTR exon 9 and its flanking sequences on diagnosis of cystic fibrosis mutations.

The Journal of molecular diagnostics : JMD - 1 Sept 2009

El-Seedy Ayman, Dudognon Tony, Bilan Frédéric, Pasquet Marie-Claude, Reboul Marie-Pierre, Iron Albert, Kitzis Alain, Ladeveze Véronique

Abstract excerpt

The DNA sequences of seven regions in the human genome were examined for sequence identity with exon 9 of the cystic fibrosis transmembrane conductance regulator (CFTR) gene, which is mutated in cystic fibrosis, and its intronic boundaries. These sequences were 95% to 96% homologous. Based on this nucleotide sequence similarity, PCR primers for CFTR exon 9 can potentially anneal with other homologous sequences in...

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Source

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Identifiers

PMID: 19710401
DOI: 10.2353/jmoldx.2009.090005
PMCID: PMC2729848

Genes

CFTR

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-07.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

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