The IVS8(n)-T variant in the CFTR gene as a factor for male infertility
نویسندگان
چکیده
منابع مشابه
Association the study of between CGA rs6631A>T gene polymorphism with the risk of male infertility
Introduction: The CGA gene encodes alpha subunit of glycoprotein hormones that are involved in the fertility process. The aim of this study was to evaluate the relationship between glycoprotein hormones, alpha polypeptide (CGA) rs6631A> T gene polymorphism with the risk of men with azoospermia or severe oligozoospermia. Methods: This study was conducted in a case-control study on 200 bloo...
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15 صفحه اولexon 10 cftr gene mutation in male infertility
background: about 10% of infertilities with obstructive azoospermia are congenital and caused by cf gene mutations. m469i mutation was observed for the first time in taiwanese patients. this mutation not only causes cf, but also may be the origin of infertility too. objective: in this study, we aimed in designing a rapid, reliable rflp-pcr procedure for detection of m469i mutation. the correlat...
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ژورنال
عنوان ژورنال: Varna Medical Forum
سال: 2020
ISSN: 2367-5519,1314-8338
DOI: 10.14748/vmf.v9i2.7210