Associated Papers
A comprehensive study of common and rare genetic variants in spermatogenesis-related loci identifies new risk factors for idiopathic severe spermatogenic failure.
Guzmán-Jiménez A et al.
Human Reproduction Open, 2024
39678461 (PubMed )
Supplement: hoae069_supplementary_data.zip › supplementary_tables.xlsx › _S13
Novel mutation in USP26 associated with azoospermia in a Sertoli cell-only syndrome patient.
Arafat M et al.
Molecular Genetics & Genomic Medicine, 2020
The impacts of nineteen mutations on the enzymatic activity of USP26.
Liu YL et al.
Gene, 2018
Association of USP26 haplotypes in men in Taiwan, China with severe spermatogenic defect.
Lee IW et al.
Asian Journal of Andrology, 2008
The Fanconi anemia pathway: repairing the link between DNA damage and squamous cell carcinoma.
Romick-Rosendale LE et al.
Mutation Research, 0
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