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
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