Identification of a heterozygous variant of ZP2 as a novel cause of empty follicle syndrome in humans and mice.
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DOI: 10.1093/humrep/deac026
Abstract: STUDY QUESTION Is a recurrent heterozygous mutation in ZP2, c.1925G>A (p.R642Q), associated with the Empty follicle syndrome (EFS)? SUMMARY ANSWER ZP2, c.1925G>A (p.R642Q), led to female infertility related to EFS in humans and mice and… read more here.
Keywords: mutation zp2; zp2r642q; mice; zp2 ... See more keywords