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Association between polymorphisms in CXCR2 gene and preeclampsia
BACKGROUND: Preeclampsia is a serious pregnancy‐specific syndrome with incompletely understood pathogenesis. Previous study has demonstrated that the decreased CXCR2 in preeclamptic placentas may contribute to the development of preeclampsia. The role of single nucleotide polymorphisms (SNPs) of CXC...
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| Publicado no: | Mol Genet Genomic Med |
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| Main Authors: | , , , , , , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
John Wiley and Sons Inc.
2019
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC6465673/ https://ncbi.nlm.nih.gov/pubmed/30714340 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1002/mgg3.578 |
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