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The Aurora Kinase C c.144delC mutation causes meiosis I arrest in men and is frequent in the North African population.

Klaus Dieterich , Raoudha Zouari , Radu Harbuz , François Vialard , Delphine Martinez , et al.
Human Molecular Genetics, 2009, 18 (7), pp.1301-9. ⟨10.1093/hmg/ddp029⟩
Journal articles inserm-00410300v1

Creation of a registry for human embryonic stem cells carrying an inherited defect: joint collaboration between ESHRE and hESCreg.

Karen D. Sermon , Carlos Simon , Peter Braude , Stéphane Viville , Joeri Borstlap , et al.
Human Reproduction, 2009, 24 (7), pp.1556-60. ⟨10.1093/humrep/dep062⟩
Journal articles inserm-00420105v1
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A recurrent deletion of DPY19L2 causes infertility in man by blocking sperm head elongation and acrosome formation.

Radu Harbuz , Raoudha Zouari , Virginie Pierre , Mariem Ben Khelifa , Mahmoud Kharouf , et al.
American Journal of Human Genetics, 2011, 88 (3), pp.351-61. ⟨10.1016/j.ajhg.2011.02.007⟩
Journal articles inserm-00588067v1