No evidence for mutations in NLRP7, NLRP2 or KHDC3L in women with unexplained recurrent pregnancy loss or infertility.
Human reproduction (Oxford, England) 2015 Jan 30 (1): 232-8.
Aghajanova L, Mahadevan S, Altmäe S, Stavreus-Evers A, Regan L, Sebire N, Dixon P, Fisher R A, Van den Veyver I
Maternal NLRP7 and C6orf221 variants are not a common risk factor for androgenetic moles, triploidy and recurrent miscarriage.
Molecular human reproduction 2013 Aug 19 (8): 539-44.
Manokhina I, Hanna C W, Stephenson M D, McFadden D E, Robinson W