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Article

Identification of a new DPY19L2 mutation and a better definition of DPY19L2 deletion breakpoints leading to globozoospermia.

Molecular human reproduction - 1 Jan 2016

Ghédir Houda, Ibala-Romdhane Samira, Okutman Ozlem, Viot Géraldine, Saad Ali, Viville Stéphane

Abstract excerpt

STUDY HYPOTHESIS: The purpose of this study was to analyze DPY19L2 sequence variants to investigate the mechanism leading to the entire DPY19L2 deletion in a large cohort of infertile globozoospermic patients. STUDY FINDING: An improved analysis of the DPY19L2 deletion breakpoints (BPs) allowed us to identify two BPs located in a small 1 kb region and to more precisely localize the BPs reported previously. WHAT...

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Source

Identifiers

PMID: 26516168
DOI: 10.1093/molehr/gav061

Genes

PICK1
SPATA16
PRKCA

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PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-07.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

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Identification of a new DPY19L2 mutation and a better definition of DPY19L2 deletion breakpoints leading to globozoospermia.PMID 26516168Read ↗

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