Srpski Arhiv za Celokupno Lekarstvo (Jan 2002)

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

  • Kušić Jelena S.,
  • Radojković Dragica P.,
  • Maletić-Vukotić Vinka D.,
  • Branković Snežana,
  • Savić Ana P.

DOI
https://doi.org/10.2298/SARH0202001K
Journal volume & issue
Vol. 130, no. 1-2
pp. 1 – 6

Abstract

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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.

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