Potensi Mutan Δf 508-T Gen Pengkode Cystic Fibrosis Transmembrane Conductance Regulator (Cftr) Sebagai Prototype Pada Penyakit Congenital Bilateral Absence Of Vas Deferens (Cbavd) Di Indonesia
CBAVD is congenital defect, data concerning the report of CBAVD case have not been reporting in Indonesia. The aim of this research to determine potency mutan ΔF 508-T gene CFTR could be used as prototype for therapy congenital defect CBAVD in Indonesia. Blood sample from Azoospermi man was collec...
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