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 between ubiquitin-specific protease USP26 polymorphism and male infertility in Chinese men.
Shi YC et al.
Clinica Chimica Acta; International Journal of Clinical Chemistry, 2011
[Mutation of the USP26 gene in spermatogenesis dysfunction].
Wei L et al.
Zhonghua Nan Ke Xue = National Journal of Andrology, 2010
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