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

• Main Author: Maslichah Mafruchati
• Format: Theses and Dissertations NonPeerReviewed
• Language: Indonesian; Indonesian; Indonesian; Indonesian; Indonesian; Indonesian; Indonesian; Indonesian; Indonesian; Indonesian
• Published: 2015
• Subjects: R735-854 Medical education. Medical schools. Research
• Online Access: http://repository.unair.ac.id/63550/1/1.%20HALAMAN%20JUDUL.pdf; http://repository.unair.ac.id/63550/2/2.%20ABSTRAK.pdf; http://repository.unair.ac.id/63550/3/3.%20BAB%201.pdf; http://repository.unair.ac.id/63550/4/4.%20BAB%202.pdf; http://repository.unair.ac.id/63550/5/5.%20BAB%203.pdf; http://repository.unair.ac.id/63550/6/6.%20BAB%204.pdf; http://repository.unair.ac.id/63550/7/7.%20BAB%205.pdf; http://repository.unair.ac.id/63550/8/8.%20BAB%206.pdf; http://repository.unair.ac.id/63550/9/9.%20BAB%207.pdf; http://repository.unair.ac.id/63550/10/10.%20DAFTAR%20PUSTAKA.pdf; http://repository.unair.ac.id/63550/; http://lib.unair.ac.id
• Institution: Universitas Airlangga

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...