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Molecular mechanism of copper transport in Wilson disease.
Fatemi N, Sarkar B. Fatemi N, et al. Environ Health Perspect. 2002 Oct;110 Suppl 5(Suppl 5):695-8. doi: 10.1289/ehp.02110s5695. Environ Health Perspect. 2002. PMID: 12426114 Free PMC article. Review.
KH domain containing 3 like (KHDC3L) frame-shift mutation causes both recurrent pregnancy loss and hydatidiform mole.
Fatemi N, Ray PF, Ramezanali F, Shahani T, Amiri-Yekta A, Kherraf ZE, Cazin C, Almadani N, Varkiani M, Sarmadi S, Sodeifi N, Gourabi H, Biglari A, Totonchi M. Fatemi N, et al. Eur J Obstet Gynecol Reprod Biol. 2021 Feb 10;259:100-104. doi: 10.1016/j.ejogrb.2021.02.006. Online ahead of print. Eur J Obstet Gynecol Reprod Biol. 2021. PMID: 33639414
Biallelic variant in cyclin B3 is associated with failure of maternal meiosis II and recurrent digynic triploidy.
Fatemi N, Salehi N, Pignata L, Palumbo P, Cubellis MV, Ramazanali F, Ray P, Varkiani M, Reyhani-Sabet F, Biglari A, Sparago A, Acurzio B, Palumbo O, Carella M, Riccio A, Totonchi M. Fatemi N, et al. J Med Genet. 2020 Sep 16:jmedgenet-2020-106909. doi: 10.1136/jmedgenet-2020-106909. Online ahead of print. J Med Genet. 2020. PMID: 32938693 Free article.
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