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)

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

Original languageEnglish
Pages (from-to)1021-1024
Number of pages4
JournalCirculation
Volume142
Issue number10
DOIs
Publication statusPublished - 8 Sep 2020

Keywords

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

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