Rare variants in genes coding for components of the terminal pathway of the complement system in preeclampsia.


Journal

Research square
Titre abrégé: Res Sq
Pays: United States
ID NLM: 101768035

Informations de publication

Date de publication:
02 Apr 2024
Historique:
medline: 22 4 2024
pubmed: 22 4 2024
entrez: 22 4 2024
Statut: epublish

Résumé

Preeclampsia is a common multifactorial disease of pregnancy. Dysregulation of the complement activation is among emerging candidates responsible for disease pathogenesis. In a targeted exomic sequencing study we identified 14 variants within nine genes coding for components of the membrane attack complex (MAC, C5b-9) that are associated with preeclampsia. We found two rare missense variants in the

Identifiants

pubmed: 38645143
doi: 10.21203/rs.3.rs-4121735/v1
pmc: PMC11030519
pii:
doi:

Types de publication

Preprint

Langues

eng

Auteurs

Classifications MeSH