Whole Exome Sequencing Identifies a Rare CFTR Mutation in Brothers With Anomalies of the Vas Deferens: A Case Study-Reference-Cited by-同舟云学术

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Whole Exome Sequencing Identifies a Rare CFTR Mutation in Brothers With Anomalies of the Vas Deferens: A Case Study

Published:2023-05 Issue: Volume:175 Page:74-76
ISSN:0090-4295
Container-title:Urology
language:en
Short-container-title:Urology

Author:

Campbell Katherine^ORCID,Dullea Alexandra,Schuppe Kyle,Ghomeshi Armin,Ramsoomair Christian,Griswold Anthony J.,Khodamoradi Kajal,Ramasamy Ranjith^ORCID

Funder

National Institute of Diabetes and Digestive and Kidney Diseases

Cystic Fibrosis Foundation

National Institutes of Health

Publisher

Elsevier BV

Subject

Urology

Reference16 articles.

1. Vasectomy, vas ligation and vas occlusion;Klapproth;Urology,1973

2. Genetics of the congenital absence of the vas deferens;Bieth;Hum Genet,2021

3. Mutations in the cystic fibrosis gene in patients with congenital absence of the vas deferens;Chillon;N Engl J Med,1995

4. Genetic, andrological and clinical characteristics of patients with congenital bilateral absence of the vas deferens;Attardo;Int J Androl,2001

5. How do we counsel men with obstructive azoospermia due to CF mutations?-A review of treatment options and outcomes;Persily;Transl Androl Urol,2021

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