No evidence for mutations in NLRP7, NLRP2 or KHDC3L in women with unexplained recurrent pregnancy loss or infertility

STUDY QUESTION: Are mutations in NLRP2/7 (NACHT, LRR and PYD domains-containing protein 2/7) or KHDC3L (KH Domain Containing 3 Like) associated with recurrent pregnancy loss (RPL) or infertility? SUMMARY ANSWER: We found no evidence for mutations in NLRP2/7 or KHDC3L in unexplained RPL or infertilit...

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Dettagli Bibliografici
Pubblicato in:Hum Reprod
Autori principali: Aghajanova, L., Mahadevan, S., Altmäe, S., Stavreus-Evers, A., Regan, L., Sebire, N., Dixon, P., Fisher, R.A., Van den Veyver, I.B.
Natura: Artigo
Lingua:Inglês
Pubblicazione: Oxford University Press 2015
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Original Articles
Accesso online:https://ncbi.nlm.nih.gov/pmc/articles/PMC4262469/
https://ncbi.nlm.nih.gov/pubmed/25376457
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1093/humrep/deu296
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