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Burden of rare exome sequence variants in PROC gene is associated with venous thromboembolism: a population-based study.

Weihong TangMary Rachel StimsonSaonli BasuSusan R HeckbertAndrea N EdgintonJames S PankowAaron R FolsomNathan Pankratz
Published in: Journal of thrombosis and haemostasis : JTH (2019)
Rare coding variants in PROC contribute to increased VTE risk in EAs in this general population sample.
Keyphrases
  • venous thromboembolism
  • copy number
  • direct oral anticoagulants
  • genome wide
  • dna methylation
  • gene expression
  • transcription factor