Article ID | Journal | Published Year | Pages | File Type |
---|---|---|---|---|
5689540 | European Journal of Obstetrics & Gynecology and Reproductive Biology | 2017 | 14 Pages |
Abstract
Our findings speculate that the FASL-844C/T polymorphism is associated with the risk of male infertility and this variation can be considered as a genetic risk factor for idiopathic azoospermia among Western Iranian men population. Summing up, these data indicated that the genetic variations in FAS/FASL system have a critical role in spermatogenesis defects and subsequent male infertility.
Keywords
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Authors
Rezvan Asgari, Kamran Mansouri, Mitra Bakhtiari, Ali Bidmeshkipour, Kheirollah Yari, Farhad Shaveisi-Zadeh, Asad Vaisi-Raygani,