Enrichment of Rare Variants in Loeys-Dietz Syndrome Genes in Spontaneous Coronary Artery Dissection but Not in Severe Fibromuscular Dysplasia
- Resource Type
- Authors
- Verstraeten, A; Perik, MHAM; Baranowska, AA; Meester, JAN; Van Den Heuvel, L; Bastianen, J; Kempers, M; Krapels, IPC; Maas, A; Rideout, A; Vandersteen, A; Sobey, G; JOHNSON, D; Fransen, E; Ghali, N; Webb, T; Al-Hussaini, A; de Leeuw, P; Delmotte, P; Lopez-Sublet, M; Pappaccogli, M; Sprynger, M; Toubiana, L; European/International Fibromuscular Dysplasia Registry and Initiative, (FEIRI); Van Laer, L; Van Dijk, FS; Vikkula, M; Samani, NJ; Persu, A; Adlam, D; Loeys, B; Collaborators of the European/International Fibromuscular Dysplasia Registry and Initiative, (FEIRI)
- Source
- Circulation
Circulation, 2020, 142, pp.1021-1024
- Subject
- fibromuscular dysplasia
genetics
[INFO.INFO-BI]Computer Science [cs]/Bioinformatics [q-bio.QM]
Loeys-Dietz syndrome
coronary artery disease
- Language
- English