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Functional FOXC1 variants in familial and sporadic atrial septal defect with cellular and animal validation.

Huan-Xin ChenHai-Tao HouXiu-Li WangJun WangQin YangGuo-Wei He
Published in: Clinical and translational medicine (2024)
Keyphrases
  • late onset
  • early onset
  • copy number
  • atrial fibrillation
  • left atrial
  • amyotrophic lateral sclerosis
  • catheter ablation
  • heart failure
  • gene expression
  • dna methylation