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   <subfield code="a">10.1007/s10815-011-9632-7</subfield>
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   <subfield code="a">(NATIONALLICENCE)springer-10.1007/s10815-011-9632-7</subfield>
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   <subfield code="a">The prevalence of common CFTR mutations in Iranian infertile men with non-CAVD obstructive azoospermia by using ARMS PCR techniques</subfield>
   <subfield code="h">[Elektronische Daten]</subfield>
   <subfield code="c">[Kyumars Safinejad, Mojtaba Darbouy, Sayed Kalantar, Sirus Zeinali, Reza Mirfakhraie, Leila Yadegar, Masoud Houshmand]</subfield>
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   <subfield code="a">Purpose: To evaluate five common cystic fibrosis trans-membrane conductance regulator (CFTR) mutations (ΔF508, G542X, R117H, W1282X and N1303K) in the Iranian infertile men with noncongenital absence of vas deferens (CAVD) obstructive azoospermia. Methods: The common CFTR gene mutations were tested on blood samples from 53 infertile men with non-CAVD obstructive azoospermia and 50 normal men as control individuals. Genomic DNA is extracted from the whole blood and the common CFTR mutations have been detected by the amplification refractory mutation system (ARMS) techniques. Results: The common CFTR mutations were found positive in 5/53)9.43%(for ΔF508 and 4/53)7.55%(for G542X mutation of all patients tested. Also, no CFTR mutations were detected in the normal men. Conclusion: The common CFTR mutations were detected in 9/53(17%) infertile men with non-CAVD obstructive azoospermia. Pre-treatment CFTR mutation analysis remains critical to distinguish cystic fibrosis (CF) genotypes for men with non CAVD obstructive azoospermia.</subfield>
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   <subfield code="a">Obstructive azoospermia</subfield>
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   <subfield code="a">Common CFTR gene mutations</subfield>
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   <subfield code="u">Research &amp; Clinical Centre for Infertility, Shahid Sadoughi Medical Sciences University Yazd, Yazd, Iran</subfield>
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   <subfield code="t">Journal of Assisted Reproduction and Genetics</subfield>
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