Association of the single nucleotide polymorphism C1858T of the PTPN22 gene with unexplained recurrent pregnancy loss: A case-control study.

Fateme KhanbarariNasrin GhasemiMahmood VakiliMorteza Samadi

Published in: International journal of reproductive biomedicine (2021)

Our findings suggest that the PTPN22 1858T polymorphism could play a role in recurrent pregnancy loss. Therefore, genotyping of the mentioned polymorphism can help clinicians to predict the probable risk of URPL.

Keyphrases

preterm birth
genome wide
pregnancy outcomes
palliative care
high throughput
dna methylation
pregnant women
gene expression
genetic diversity