Angiotensin, transforming growth factor β and aortic dilatation in Marfan syndrome: Of mice and humans
Marfan syndrome is consequent upon mutations in FBN1, which encodes the extracellular matrix microfibrillar protein fibrillin-1. The phenotype is characterised by development of thoracic aortic aneurysm. Current understanding of the pathogenesis of aneurysms in Marfan syndrome focuses upon abnormal...
Main Authors: | , |
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Format: | Article |
Language: | English |
Published: |
Elsevier
2018-03-01
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Series: | International Journal of Cardiology: Heart & Vasculature |
Online Access: | http://www.sciencedirect.com/science/article/pii/S2352906717300714 |