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Genome-wide Epistasis for Cardiovascular Severity in Marfan Study

University Hospital, Antwerp · 2020
ClinicalTrials.gov · Datasets · License: Public Domain · 2020
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marfan syndrome, fbn1 mutation, p.ile2585thr;c.7754t>c, rare disease, aortopathies, taad, congenital abnormalities, genetic modifiers, thoracic aortic disease, thoracic aortic rupture, observational
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