Whole exome sequencing identifies a new DPY19L2 variant c.1232_1233insA in Tunisian infertile patient with globozoospermia

Whole exome sequencing identifies a new DPY19L2 variant c.1232_1233insA in Tunisian infertile patient with globozoospermia

Abstract Background Globozoospermia is a rare male infertility disorder characterized by the presence in the ejaculate of round-headed sperm cells lacking an acrosome, a crucial structure for fertilization. While genetic factors play a significant role in the etiology of this condition, the precise...

Full description

Saved in:
Bibliographic Details
Main Authors: Wiem Ayed, Nicolas Thierry-Mieg, Wajh Hammami, Meriem Ben Khalifa, Sonia Mnallah, Hanène Eloumi, Amel Zhioua, Anis Chaker, Fethi Zhioua, Pierre F. Ray, Ahlem Amouri
Format: Article
Language:English
Published: SpringerOpen 2025-07-01
Series:Middle East Fertility Society Journal
Subjects:
Male infertility
Globozoospermia
DPY19L2
Whole exome sequencing
Online Access:https://doi.org/10.1186/s43043-025-00235-8
Tags: Add Tag
No Tags, Be the first to tag this record!

Internet

https://doi.org/10.1186/s43043-025-00235-8

Similar Items