P292: Contribution of rare variants in the development of familial premature coronary artery disease in a cohort of cardiac patients

Gespeichert in:

Autor*in:	Sepideh Mehvari [verfasserIn] Nahid Karimian Fathi [verfasserIn] Maryam Asadnezhad [verfasserIn] Sanaz Arzhangi [verfasserIn] Saeed Sadeghian [verfasserIn] Mohammadali Boroumand [verfasserIn] Fatemeh Shokohizadeh [verfasserIn] Elham Rostami [verfasserIn] Rahnama Boroumand [verfasserIn] Reza Malekzadeh [verfasserIn] Yasser Riazalhosseini [verfasserIn] Mohammadreza Akbari [verfasserIn] Mark Lathrop [verfasserIn] Hossein Najmabadi [verfasserIn] Kaveh Hosseini [verfasserIn] Kimia Kahrizi [verfasserIn]

Format:	E-Artikel
Sprache:	Englisch

Erschienen:	2024

Übergeordnetes Werk:	In: Genetics in Medicine Open ; 2(2024), Seite 101188- volume:2 ; year:2024 ; pages:101188-

Links:	Link aufrufen Link aufrufen Link aufrufen Journal toc

DOI / URN:	10.1016/j.gimo.2024.101188

Katalog-ID:	DOAJ095605363

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P292: Contribution of rare variants in the development of familial premature coronary artery disease in a cohort of cardiac patients

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