Exome sequencing reveals SYCE1 mutation associated with autosomal recessive primary ovarian insufficiency.de Vries L., Behar D.M., Smirin-Yosef P., Lagovsky I., Tzur S., Basel-Vanagaite L.View abstractCited forINVOLVEMENT IN POF12CategoriesDisease & VariantsSourceUniProtKB reviewed (Swiss-Prot)PubMedEurope PMCJ. Clin. Endocrinol. Metab. 99:E2129-E2132 (2014)Cited in1Mapped to1
Deleterious mutation in SYCE1 is associated with non-obstructive azoospermia.Maor-Sagie E., Cinnamon Y., Yaacov B., Shaag A., Goldsmidt H., Zenvirt S., Laufer N., Richler C., Frumkin A.View abstractCited forINVOLVEMENT IN SPGF15CategoriesDisease & VariantsSourceUniProtKB reviewed (Swiss-Prot)PubMedEurope PMCJ. Assist. Reprod. Genet. 32:887-891 (2015)Cited in1