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Article

HRG C633T polymorphism and risk of gestational hypertensive disorders: a pilot study.

BMC medical genetics - 14 Mar 2018

Elenis Evangelia, Skalkidou Alkistis, Skoog-Svanberg Agneta, Sydsjö Gunilla, Stavreus-Evers Anneli, Åkerud Helena

Abstract excerpt

BACKGROUND: Preeclampsia and gestational hypertensive disorders are thought to occur due to endothelial cell dysfunction and abnormal placentation, triggered by angiogenesis-related factors yet undetermined. The aim of this study was to investigate whether a genetic polymorphism (SNP) of Histidine-rich glycoprotein (HRG), HRG C633T SNP, is associated with gestational hypertensive disorders. METHODS: It was...

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Identifiers

PMID: 29540166
DOI: 10.1186/s12881-018-0550-8
PMCID: PMC5853153

Genes

HRG

Variants

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PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-07.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

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