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:: Volume 15, Issue 4 (تابستان 1393: 15 (4) 1393) ::
Koomesh 1393, 15(4): 431-440 Back to browse issues page
Cystic fibrosis anddistribution and mutation analysis of CFTR gene in Iranian patients
Mohammad Reza Havasian, Jafar Panahi, Nejat Mahdieh *
Abstract:   (7735 Views)
 Cystic fibrosis is one of the most lethal multi-system disorders and is the most common autosomal recessive disease in Caucasians. The related protein is named cystic fibrosis transmembrane conductive regulator (CFTR). Various mutations in CFTR gene have been reported to cause CFTR loss of function and diseased phenotype. The most prevalent mutation is ΔF508, deletion of phe at position 508. Here, we briefly explain clinical features and diagnostic methods of the disease firstly, and then the genetics of the disease and its mutations as well as genetic studies in Iranian populations are reviewed. Up to now, totally 56 different mutations have been reported in Iranian patients which 8 of them reported for the first time. Seven common mutations in this population are as follows p.F508del (33.33%), c.1677delTA (7.41%), c.2183_2184delAAinsG (5.56%), p.N1303K (4.81%), c.2789+5G>A (4.44%), p.S466X (4.44%) and p.G542X (4.07%). 
Keywords: Cystic fibrosis, CFTR, Iranian population
Full-Text [PDF 336 kb]   (8776 Downloads)    
Type of Study: Review | Subject: General
Received: 2013/09/25 | Accepted: 2014/01/21 | Published: 2014/06/11
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Havasian M R, Panahi J, Mahdieh N. Cystic fibrosis anddistribution and mutation analysis of CFTR gene in Iranian patients. Koomesh 1393; 15 (4) :431-440
URL: http://koomeshjournal.semums.ac.ir/article-1-2226-en.html


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Volume 15, Issue 4 (تابستان 1393: 15 (4) 1393) Back to browse issues page
کومش Koomesh
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