CFTR gene mutation spectrum among 735 Iranian patients with cystic fibrosis: A comprehensive systematic review.

doi:10.1002/ppul.25647

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Article

CFTR gene mutation spectrum among 735 Iranian patients with cystic fibrosis: A comprehensive systematic review.

Pediatric pulmonology - 1 Dec 2021

Alibakhshi Reza, Mohammadi Aboozar, Khamooshian Sahand, Kazeminia Mohsen, Moradi Keivan

Abstract excerpt

In this study, the spectrum and frequency of cystic fibrosis transmembrane conductance regulator (CFTR) gene mutations previously reported among Iranian cystic fibrosis (CF) patients have been reviewed and discussed. Using the keywords of Cystic Fibrosis, CF, CFTR, and Iran, along with their Persian equivalents, a comprehensive search was performed on the online databases. After applying the inclusion and...

Topics

Cystic Fibrosis
Cystic Fibrosis Transmembrane Conductance Regulator
Humans
Iran
Mutation

Source

Open in PubMed

Identifiers

PMID: 34525262
DOI: 10.1002/ppul.25647

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PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 30 Aug 2026.

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