Article

The heterozygous mutations of SLC26A8 are not the main actors but might be the guest players for male infertility

2021-11-20

Abstract excerpt

Male infertility has become a serious health and social problem troubling approximately 15% of couples worldwide; however, the genetic and phenotypic heterogeneity of human infertility poses a substantial obstacle to effective diagnosis and therapy. A previous study reported that heterozygous mutations in solute carrier family 26 member 8 (SLC26A8, NG_033897.1) were causatively linked to asthenozoospermia. Interes...

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Literature Corpus work: 0c4b1f50-5ee1-5482-be4b-da1bcd19f0db
DOI: 10.22541/au.163742087.72794379/v1

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