Associated Papers
Summarizing the human genes and their variants causative of non-obstructive azoospermia uncovered using whole genome/exome sequencing.
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Reproductive Biology, 2025
A systematic review on the genetics of male infertility in the era of next-generation sequencing.
Robay A et al.
Arab Journal of Urology, 2018
Whole-exome sequencing identifies novel homozygous mutation in NPAS2 in family with nonobstructive azoospermia.
Ramasamy R et al.
Fertility and Sterility, 2015
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