Screening of mutations and polymorphism in CFRT gene in men infertile due to oligo- or azospermia

Abstract

We concluded that CFTR gene plays a role in the etiology of obstructive azoospermia and that it also could be involved in same cases of impaired spermatogenesis and sperm maturation. Due to the high incidence of CFRT mutations in patients with obstructive azoospermia we suggest screening of CFRT mutations before assisted reproduction

    Similar works

    Full text

    thumbnail-image