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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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| Publicado no: | Medicine (Baltimore) |
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| Main Authors: | , , , , , , , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
Wolters Kluwer Health
2019
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC6708840/ https://ncbi.nlm.nih.gov/pubmed/30896667 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1097/MD.0000000000014954 |
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