Associated Papers
Summarizing the human genes and their variants causative of non-obstructive azoospermia uncovered using whole genome/exome sequencing.
Ibrahim R et al.
Reproductive Biology, 2025
Whole-exome sequencing identifies rare recessive variants in azoospermia patients from consanguineous Pakistani families.
Uddin I et al.
Molecular Genetics and Genomics : Mgg, 2024
Association of ESX1 gene variants with non-obstructive azoospermia in Chinese males.
Ma Q et al.
Scientific Reports, 2021
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