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To describe in vitro development of human embryos derived from an individual with a homozygous pathogenic variant in NLRP7 (19q13.42) and recurrent hydatidiform mole (HM), an autosomal recessive condition thought to occur secondary to an oocyte defect.

daehan saengsik uihak hoeji/clinical and experimental reproductive medicine

Pathogenic variant in <i>NLRP7</i> (19q13.42) associated with recurrent gestational trophoblastic disease: Data from early embryo development observed during <i>in vitro</i> fertilization

Pathogenic variant in NLRP7 (19q13.42) associated with recurrent gestational trophoblastic disease: Data from early embryo development observed during in vitro fertilization