Associated Papers
Biallelic NLRP7 variants in patients with recurrent hydatidiform mole: A review and expert consensus.
Slim R et al.
Human Mutation, 2022
NLRP7: From inflammasome regulation to human disease.
Carriere J et al.
Immunology, 2021
Pathogenic variant in NLRP7 (19q13.42) associated with recurrent gestational trophoblastic disease: Data from early embryo development observed during in vitro fertilization.
Sills ES et al.
Clinical and Experimental Reproductive Medicine, 2017
Screening for NLRP7 mutations in familial and sporadic recurrent hydatidiform moles: report of 2 Tunisian families.
Landolsi H et al.
International Journal of Gynecological Pathology : Official Journal of the International Society of Gynecological Pathologists, 2011
Identification of 13 novel NLRP7 mutations in 20 families with recurrent hydatidiform mole; missense mutations cluster in the leucine-rich region.
Wang CM et al.
Journal of Medical Genetics, 2009
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