Enrichment of Rare Variants in Loeys–Dietz Syndrome Genes in Spontaneous Coronary Artery Dissection but Not in Severe Fibromuscular Dysplasia
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| Veröffentlicht in: | Circulation (New York, N.Y.) N.Y.), 2020-09, Vol.142 (10), p.1021-1024 |
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| container_title | Circulation (New York, N.Y.) |
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| creator | Verstraeten, Aline Perik, Melanie H.A.M. Baranowska, Anna A. Meester, Josephina A.N. Van Den Heuvel, Lotte Bastianen, Jarl Kempers, Marlies Krapels, Ingrid P.C. Maas, Angela Rideout, Andrea Vandersteen, Anthony Sobey, Glenda Johnson, Diana Fransen, Erik Ghali, Neeti Webb, Tom Al-Hussaini, Abtehale de Leeuw, Peter Delmotte, Philippe Lopez-Sublet, Marilucy Pappaccogli, Marco Sprynger, Muriel Toubiana, Laurent Van Laer, Lut Van Dijk, Fleur S. Vikkula, Miikka Samani, Nilesh J. Persu, Alexandre Adlam, David Loeys, Bart |
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| doi_str_mv | 10.1161/CIRCULATIONAHA.120.045946 |
| format | Article |
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| fulltext | fulltext |
| identifier | ISSN: 0009-7322 |
| ispartof | Circulation (New York, N.Y.), 2020-09, Vol.142 (10), p.1021-1024 |
| issn | 0009-7322 1524-4539 |
| language | eng |
| recordid | cdi_hal_primary_oai_HAL_hal_03467687v1 |
| source | American Heart Association Journals; EZB-FREE-00999 freely available EZB journals; Journals@Ovid Complete |
| subjects | Bioinformatics Computer Science |
| title | Enrichment of Rare Variants in Loeys–Dietz Syndrome Genes in Spontaneous Coronary Artery Dissection but Not in Severe Fibromuscular Dysplasia |
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