ArticleFrontiers in cell and developmental biology2026
A novel frameshift variant in
Article in Frontiers in cell and developmental biology, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.
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Abstract
Background: Severe sperm motility defects are an important cause of male infertility and are frequently associated with sperm flagellar abnormalities. Methods: A Chinese man with total asthenozoospermia was investigated using whole-exome sequencing, Sanger sequencing, transmission electron microscopy, sperm immunofluorescence, and heterologous expression analysis in HEK293 T cells. The clinical outcome following intracytoplasmic sperm injection (ICSI) was also evaluated. Results: Whole-exome sequencing identified a novel Conclusion: We identified a novel
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