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Author

Mohammadreza Dehghani

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Open access Jul 2026

Identification of novel variants in SSX1, CPNE1, and SPTBN5 in men with oligoasthenoteratozoospermia using whole-genome sequencing.

Rare candidate variants in SSX1, CPNE1, and SPTBN5 that may potentially be associated with the molecular basis of oligoasthenoteratozoospermia are identified and support the application of WGS in unresolved male infertility.

Sara Sadeghzadeh, A. Malcher, Razieh Ebrahimi Askari et al. · 0 citations

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