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CFTR Exon 10 deleterious mutations in patients with congenital bilateral absence of vas deferens in a cohort of Pakistani patients.

Archivio italiano di urologia, andrologia : organo ufficiale [di] Societa italiana di ecografia urologica e nefrologica - 2 Oct 2024

Bakhat Khush, Mateen Irsa, Saif Hina, Anwar Kanwal, Sarfraz Sadaf, Javaid Sheza, Ur Rehman Khaleeq, Arshad Adnan, Mustafa Muhammad

Abstract excerpt

Congenital bilateral absence of vas deferens (CBAVD) is a urological syndrome of Wolffian ducts and is responsible for male infertility and obstructive azoospermia. This study is designed to explore the integrity of exon 10 of CFTR and its role in male infertility in a cohort of CBVAD patients in Pakistan. Genomic DNA was extracted from 17 male patients with CBAVD having clinical symptoms, and 10 healthy controls...

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PMID: 39356031
DOI: 10.4081/aiua.2024.12464

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PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 3 Sept 2026.

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