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Further exploration of cardiac channelopathy and cardiomyopathy genes in stillbirth.

Maja Dolanc MercUrška KotnikBorut PeterlinLuca Lovrecic
Published in: Prenatal diagnosis (2024)
Several potentially stillbirth-related genetic variants were detected in our cohort, adding to the growing literature on cardiac phenotype gene variation in stillbirth. However, the mechanisms of action, gene-gene interaction, and contribution of the uterine environment are still to be deciphered. In order to advance our knowledge of the genetics of unexplained fetal death, there is an evident need for international collaboration and field standardization.
Keyphrases
  • genome wide
  • genome wide identification
  • copy number
  • healthcare
  • systematic review
  • heart failure
  • genome wide analysis
  • dna methylation