P292: Contribution of rare variants in the development of familial premature coronary artery disease in a cohort of cardiac patients
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] |
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Format: |
E-Artikel |
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Sprache: |
Englisch |
Erschienen: |
2024 |
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Übergeordnetes Werk: |
In: Genetics in Medicine Open ; 2(2024), Seite 101188- volume:2 ; year:2024 ; pages:101188- |
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Links: |
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DOI / URN: |
10.1016/j.gimo.2024.101188 |
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Katalog-ID: |
DOAJ095605363 |
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