Article

Loss-of-Function SPAG17 Variant in Patients with Severe Asthenozoospermia: Upgrading Gene-Disease Validity to Moderate

2025-03-03

Abstract excerpt

<title>Abstract</title> <p>Severe asthenozoospermia is a significant cause of male infertility, commonly associated with genetic defects affecting sperm motility. However, the specific genetic contributors remain underexplored. This study aimed to identify a genetic variant responsible for severe asthenozoospermia in two siblings and to evaluate the clinical validity of the gene-disease relationship between <ital...

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Literature Corpus work: 3621d73a-ec77-5b9b-b40e-0fc3472a8269
DOI: 10.21203/rs.3.rs-6046882/v1

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Loss-of-Function SPAG17 Variant in Patients with Severe Asthenozoospermia: Upgrading Gene-Disease Validity to ModerateDOI 10.21203/rs.3.rs-6046882/v1Read

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