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Article

Novel CFTR Mutations in Two Iranian Families with Severe Cystic Fibrosis.

Iranian biomedical journal - 1 Sept 2016

Mohseni Marzieh, Razzaghmanesh Mohammad, Parsi Mehr Elham, Zare Hanieh, Beheshtian Maryam, Najmabadi Hossein

Abstract excerpt

BACKGROUND: Cystic fibrosis (CF) is a common autosomal recessive disorder that affects many body systems and is produced by mutations in the cystic fibrosis transmembrane conductance regulator (CFTR) gene. CF is also the most frequently inherited disorder in the West. The aim of this study was to detect the mutations in the CFTR gene in two Iranian families with CF. METHODS: After DNA extraction using the salting...

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Identifiers

PMID: 27017198
DOI: 10.7508/ibj.2016.04.003
PMCID: PMC4983674

Genes

CFTR

Variants

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Source receipt: pubmed, retrieved 7 Sept 2026.

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