Association between RUNX3 gene polymorphisms in severe preeclampsia and its clinical features

Preeclampsia is a complex genetic disorder and its pathogenesis remains to be investigated. Single nucleotide polymorphisms serve important roles in genetic predisposition. The present study aimed to explore the association between runt-related transcription factor 3 (RUNX3) gene polymorphisms in se...

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Detalles Bibliográficos
Autores principales: Zhang, Yanping, Wang, Tao, Jia, Jin, Cao, Wen, Ye, Lei, Wang, Yanyun, Zhou, Bin, Zhou, Rong
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Wolters Kluwer Health 2019
Materias:
Research Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6708840/
https://www.ncbi.nlm.nih.gov/pubmed/30896667
http://dx.doi.org/10.1097/MD.0000000000014954

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6708840/
https://www.ncbi.nlm.nih.gov/pubmed/30896667
http://dx.doi.org/10.1097/MD.0000000000014954

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