Biallelic variants in DNAH11 cause male infertility with asthenozoospermia in a Chinese non-consanguineous family: A case report
This study identified novel biallelic DNAH11 variants associated with reduced sperm motility, expanding the known mutational spectrum of DNAH11 variants implicated in AZS and providing additional evidence for genetic counseling and diagnosis.
Authors
- Huiling Qu (ORCID: https://orcid.org/0000-0003-0909-6267)
- Haiping Liu (ORCID: https://orcid.org/0009-0005-4037-4335)
- Na Shi (ORCID: https://orcid.org/0000-0003-1564-2236)
- Lu Jiang (ORCID: https://orcid.org/0000-0001-6003-7575)
- Junlin Pan (ORCID: https://orcid.org/0000-0002-2683-6223)
- Yan Zhang (ORCID: https://orcid.org/0000-0003-2031-0631)
- Jingpeng Hou (ORCID: https://orcid.org/0000-0001-5248-7103)
Institutions
- 117th Hospital of People's Liberation Army (CN)
- People's Liberation Army 401 Hospital (CN)
Publication Details
- Journal
- Medicine
- Published
- 2025-12-12
- DOI
- https://doi.org/10.1097/md.0000000000046556
- Primary Topic
- Neurological diseases and metabolism
- Type
- article
- Field-Weighted Citation Impact
- 0.00