Associated Papers
Molecular genetics of infertility: loss-of-function mutations in humans and corresponding knockout/mutated mice.
Jiao SY et al.
Human Reproduction Update, 2021
Genetic analyses of a large cohort of infertile patients with globozoospermia, DPY19L2 still the main actor, GGN confirmed as a guest player.
Celse T et al.
Human Genetics, 2021
Validation and application of a novel integrated genetic screening method to a cohort of 1,112 men with idiopathic azoospermia or severe oligozoospermia.
Oud MS et al.
Human Mutation, 2017
DPY19L2 gene mutations are a major cause of globozoospermia: identification of three novel point mutations.
Zhu F et al.
Molecular Human Reproduction, 2013
Globozoospermia is mainly due to DPY19L2 deletion via non-allelic homologous recombination involving two recombination hotspots.
Elinati E et al.
Human Molecular Genetics, 2012
Novel DPY19L2 variants in globozoospermic patients and the overcoming this male infertility.
Shang YL et al.
Asian Journal of Andrology, 0
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