Association of the PHACTR1/EDN1 Genetic Locus With Spontaneous Coronary Artery Dissection

Spontaneous coronary artery dissection (SCAD) is an increasingly recognized cause of acute coronary syndromes (ACS) afflicting predominantly younger to middle-aged women. Observational studies have reported a high prevalence of extracoronary vascular anomalies, especially fibromuscular dysplasia (FM...

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Vydané v:	Journal of the American College of Cardiology Ročník 73; číslo 1; s. 58
Hlavní autori:	Adlam, David, Olson, Timothy M, Combaret, Nicolas, Kovacic, Jason C, Iismaa, Siiri E, Al-Hussaini, Abtehale, O'Byrne, Megan M, Bouajila, Sara, Georges, Adrien, Mishra, Ketan, Braund, Peter S, d'Escamard, Valentina, Huang, Siying, Margaritis, Marios, Nelson, Christopher P, de Andrade, Mariza, Kadian-Dodov, Daniella, Welch, Catherine A, Mazurkiewicz, Stephani, Jeunemaitre, Xavier, Wong, Claire Mei Yi, Giannoulatou, Eleni, Sweeting, Michael, Muller, David, Wood, Alice, McGrath-Cadell, Lucy, Fatkin, Diane, Dunwoodie, Sally L, Harvey, Richard, Holloway, Cameron, Empana, Jean-Philippe, Jouven, Xavier, Olin, Jeffrey W, Gulati, Rajiv, Tweet, Marysia S, Hayes, Sharonne N, Samani, Nilesh J, Graham, Robert M, Motreff, Pascal, Bouatia-Naji, Nabila
Médium:	Journal Article
Jazyk:	English
Vydavateľské údaje:	United States 08.01.2019
Predmet:	Adult Aged Australia Case-Control Studies Coronary Vessel Anomalies - complications Coronary Vessel Anomalies - epidemiology Coronary Vessel Anomalies - genetics Endothelin-1 - genetics Female Fibromuscular Dysplasia - complications Fibromuscular Dysplasia - genetics France Genetic Loci - genetics Humans Male Microfilament Proteins - genetics Middle Aged Prevalence United Kingdom United States Vascular Diseases - complications Vascular Diseases - congenital Vascular Diseases - epidemiology Vascular Diseases - genetics United Kingdom Australia France United States cardiovascular disease in women genetic association fibromuscular dysplasia myocardial infarction
ISSN:	1558-3597, 1558-3597
On-line prístup:	Zistit podrobnosti o prístupe
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