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Case report Open access Sep 2026

Identification and splicing assessment of a novel homozygous CFAP65 splice-site variant associated with oligozoospermia and complete asthenozoospermia

Pathogenic variants in CFAP65 have been reported in male infertility with sperm motility defects. This study investigated a novel homozygous CFAP65 splice-site variant identified in a consanguineous family in which the proband presented with oligozoospermia and complete asthenozoospermia. Whole-exome sequencing was per...

Cong-Cong Teng, Xin-Hua Tang, Lin Li et al. · 0 citations

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