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Mutations Of The Cftr Gene In Turkish Patients With Congenital Bilateral Absence Of The Vas Deferens
(Oxford Univ Press, 2004)
BACKGROUND: Mutations of the Cystic Fibrosis Transmembrane Conductance Regulator (CFTR) can cause congenital bilateral absence of the vas deferens (CBAVD) as a primarily genital form of cystic fibrosis. The spectrum and ...