MP75-08 WHOLE EXOME SEQUENCING IDENTIFIES A RARE NONSENSE MUTATION IN FAM47C AS A POSSIBLE CAUSE OF SEVERE OLIGOSPERMIA IN BROTHERS WITH VARICOCELE

Journal article

Peer reviewed

Willy Chertman, Diana M Lopategui, Anthony J Griswold, Himanshu Arora and Ranjith Ramasamy

The Journal of urology, Vol.201(Supplement 4)

2019-04

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Title: MP75-08 WHOLE EXOME SEQUENCING IDENTIFIES A RARE NONSENSE MUTATION IN FAM47C AS A POSSIBLE CAUSE OF SEVERE OLIGOSPERMIA IN BROTHERS WITH VARICOCELE
Creators: Willy Chertman - MIAMI, FL;
Diana M Lopategui - MIAMI, FL;
Anthony J Griswold - MIAMI, FL;
Himanshu Arora - Miami, FL
Ranjith Ramasamy - Miami, FL
Publication Details: The Journal of urology, Vol.201(Supplement 4)
Academic Unit: Miller School of Medicine; UMMG Dept of Human Genetics (Dr. John T. Macdonald Foundation); UMMG Department of Urology; UMMG Department of Pathology
Language: English
Resource Type: Journal article
Record Identifier: 991031714193402976