Case Report: A homozygous mutation in the SPAG17 gene in a case with oligoasthenoteratozoospermic infertility
Our study identified a homozygous likely pathogenic mutation (c.4511A > G, Asn1504Ser) in the <i>SPAG17</i> gene that explains oligoasthenoteratozoospermic infertility in the present case.
Authors
- Singh Rajender (ORCID: https://orcid.org/0000-0002-4592-6566)
- Shruti Sethi (ORCID: https://orcid.org/0000-0002-2091-3048)
- Kalyan Mitra (ORCID: https://orcid.org/0000-0002-7252-1716)
- Waseem Andrabi
Institutions
- Central Drug Research Institute (IN)
- Academy of Scientific and Innovative Research (IN)
Publication Details
- Journal
- Frontiers in Reproductive Health
- Published
- 2025-04-22
- DOI
- https://doi.org/10.3389/frph.2025.1554027
- Citations
- 1
- Primary Topic
- Reproductive Biology and Fertility
- Type
- article
- Field-Weighted Citation Impact
- 1.88