Contribution of genetic variants in the development of familial premature coronary artery disease in a cohort of cardiac patients.

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作者： Sepideh,Mehvari ^[1] ; Nahid,Karimian Fathi ^[1] ; Sara,Saki ^[2] ; Maryam,Asadnezhad ^[1] ; Sanaz,Arzhangi ^[1] ; Fatemeh,Ghodratpour ^[1] ; Marzieh,Mohseni ^[1] ; Farzane,Zare Ashrafi ^[1] ; Saeed,Sadeghian ^[3] ; Mohammadali,Boroumand ^[3] ; Fatemeh,Shokohizadeh ^[3] ; Elham,Rostami ^[3] ; Rahnama,Boroumand ^[3] ; Reza,Najafipour ^[1] ; Reza,Malekzadeh ^[2] ; Yasser,Riazalhosseini ^[4] ; Mohammadreza,Akbari ^[5] ; Mark,Lathrop ^[4] ; Hossein,Najmabadi ^[1] ; Kaveh,Hosseini ^[3] ; Kimia,Kahrizi ^[1]

作者单位： Genetics Research Center, University of Social Welfare and Rehabilitation Sciences, Tehran, Iran. ^[1] Digestive Disease Research Institute, Tehran University of Medical Sciences, Tehran, Iran. ^[2] Tehran Heart Center, Cardiovascular Diseases Research Institute, Tehran University of Medical Sciences, Tehran, Iran. ^[3] McGill Genome Centre, Montreal, Quebec, Canada. ^[4] Women's College Research Institute, University of Toronto, Toronto, Ontario, Canada. ^[5]

关键词 atherosclerosis coronary artery disease myocardial infarction premature coronary artery disease rare variant