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References

1. Coutton C, Abada F, Karaouzene T, Sanlaville D, Satre V, Lunardi J, Jouk PS,Arnoult C, Thierry-Mieg N, Ray PF. Fine characterisation of a recombinationhotspot at the DPY19L2 locus and resolution of the paradoxical excess ofduplications over deletions in the general population. PLoS Genet. 2013Mar;9(3):e1003363. doi: 10.1371/journal.pgen.1003363.
2. Coutton C, Zouari R, Abada F, Ben Khelifa M, Merdassi G, Triki C, Escalier D, Hesters L, Mitchell V, Levy R, Sermondade N, Boitrelle F, Vialard F, Satre V,Hennebicq S, Jouk PS, Arnoult C, Lunardi J, Ray PF. MLPA and sequence analysis ofDPY19L2 reveals point mutations causing globozoospermia. Hum Reprod. 2012Aug;27(8):2549-58. doi: 10.1093/humrep/des160.
3. Escoffier J, Yassine S, Lee HC, Martinez G, Delaroche J, Coutton C, KaraouzèneT, Zouari R, Metzler-Guillemain C, Pernet-Gallay K, Hennebicq S, Ray PF, Fissore R, Arnoult C. Subcellular localization of phospholipase Cζ in human sperm and itsabsence in DPY19L2-deficient sperm are consistent with its role in oocyteactivation. Mol Hum Reprod. 2015 Feb;21(2):157-68. doi: 10.1093/molehr/gau098.
4. Harbuz R, Zouari R, Pierre V, Ben Khelifa M, Kharouf M, Coutton C, Merdassi G,Abada F, Escoffier J, Nikas Y, Vialard F, Koscinski I, Triki C, Sermondade N,Schweitzer T, Zhioua A, Zhioua F, Latrous H, Halouani L, Ouafi M, Makni M, JoukPS, Sèle B, Hennebicq S, Satre V, Viville S, Arnoult C, Lunardi J, Ray PF. Arecurrent deletion of DPY19L2 causes infertility in man by blocking sperm headelongation and acrosome formation. Am J Hum Genet. 2011 Mar 11;88(3):351-61. doi:10.1016/j.ajhg.2011.02.007.
5. Koscinski I, Elinati E, Fossard C, Redin C, Muller J, Velez de la Calle J,Schmitt F, Ben Khelifa M, Ray PF, Kilani Z, Barratt CL, Viville S. DPY19L2deletion as a major cause of globozoospermia. Am J Hum Genet. 2011 Mar11;88(3):344-50. doi: 10.1016/j.ajhg.2011.01.018. Erratum in: Am J Hum Genet.2011 Apr 8;88(4):517. Ray, Pierre [corrected to Ray, Pierre F].
6. Perrin A, Coat C, Nguyen MH, Talagas M, Morel F, Amice J, De Braekeleer M.Molecular cytogenetic and genetic aspects of globozoospermia: a review.Andrologia. 2013 Feb;45(1):1-9. doi: 10.1111/j.1439-0272.2012.01308.x.
7. Pierre V, Martinez G, Coutton C, Delaroche J, Yassine S, Novella C,Pernet-Gallay K, Hennebicq S, Ray PF, Arnoult C. Absence of Dpy19l2, a new inner nuclear membrane protein, causes globozoospermia in mice by preventing theanchoring of the acrosome to the nucleus. Development. 2012 Aug;139(16):2955-65. doi: 10.1242/dev.077982.
8. Yassine S, Escoffier J, Martinez G, Coutton C, Karaouzène T, Zouari R, RavanatJL, Metzler-Guillemain C, Lee HC, Fissore R, Hennebicq S, Ray PF, Arnoult C.Dpy19l2-deficient globozoospermic sperm display altered genome packaging and DNA damage that compromises the initiation of embryo development. Mol Hum Reprod.2015 Feb;21(2):169-85. doi: 10.1093/molehr/gau099.