Enrichment of Rare Variants in Loeys-Dietz Syndrome Genes in Spontaneous Coronary Artery Dissection but Not in Severe Fibromuscular Dysplasia

Aline Verstraeten, Melanie H. A. M. Perik, Anna A. Baranowska, Josephina A. N. Meester, Lotte Van Den Heuvel, Jarl Bastianen, Marlies Kempers, Ingrid P. C. Krapels, Angela Maas, Andrea Rideout, Anthony Vandersteen, Glenda Sobey, Diana Johnson, Erik Fransen, Neeti Ghali, Tom Webb, Abtehale Al-Hussaini, Peter de Leeuw, Philippe Delmotte, Marilucy Lopez-SubletMarco Pappaccogli, Muriel Sprynger, Laurent Toubiana, Lut Van Laer, Fleur S. Van Dijk, Miikka Vikkula, Nilesh J. Samani, Alexandre Persu, David Adlam*, Bart Loeys*, European/International Fibromuscular Dysplasia Registry and Initiative (FEIRI)

*Corresponding author for this work

Research output: Contribution to journalComment/Letter to the editorAcademicpeer-review

19 Citations (Web of Science)
Original languageEnglish
Pages (from-to)1021-1024
Number of pages4
Issue number10
Publication statusPublished - 8 Sep 2020


  • coronary artery disease
  • fibromuscular dysplasia
  • genetics
  • Loeys-Dietz syndrome

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