frequency of follicle stimulating hormone receptor gene polymorphisms in Iranian infertile men with azoospermia

ABSTRACT

Background: Azoospermia is the medical condition of a man not having any measurable level of sperm in his semen. Follicle stimulating hormone [FSH] is a member of the glycoprotein hormone family that plays an important role in human reproduction because of its essential role in normal spermatogenesis. Various Single Nucleotide Polymorphisms [SNPs] have been reported within FSH receptor [FSHR] gene that may affect the receptor function