Exploration of CYP21A2 and CYP17A1 polymorphisms and preeclampsia risk among Chinese Han population: a large-scale case-control study based on 5021 subjects

BACKGROUND: Several genome-wide association studies have identified single-nucleotide polymorphisms (SNPs), such as rs4409766, rs1004467, and rs3824755 in CYP17A1 and rs2021783 in CYP21A2, as new hypertension susceptibility genetic variants in the Chinese population. This study aimed to look into th...

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Detalles Bibliográficos
Autores principales: Hou, Bo, Jia, Xuewen, Deng, Ziwen, Liu, Xin, Liu, Huitang, Yu, Haichu, Liu, Shiguo
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2020
Materias:
Primary Research
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7517682/
https://www.ncbi.nlm.nih.gov/pubmed/32977860
http://dx.doi.org/10.1186/s40246-020-00286-0

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7517682/
https://www.ncbi.nlm.nih.gov/pubmed/32977860
http://dx.doi.org/10.1186/s40246-020-00286-0

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