Associated Papers
The role of SLC26A8 homozygous variants in male infertility and flagellum abnormalities.
Mao B et al.
Asian Journal of Andrology, 2024
Novel biallelic mutations in SLC26A8 cause severe asthenozoospermia in humans owing to midpiece defects: Insights into a putative dominant genetic disease.
Gao Y et al.
Human Mutation, 2022
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