Severe Molecular Defects Exhibited by the R179H Mutation in Human Vascular Smooth Muscle α-Actin
Author:
Funder
National Institutes of Health
Publisher
Elsevier BV
Subject
Cell Biology,Molecular Biology,Biochemistry
Reference36 articles.
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2. Mutations in smooth muscle α-actin (ACTA2) lead to thoracic aortic aneurysms and dissections;Guo;Nat. Genet,2007
3. Mutations in smooth muscle α-actin (ACTA2) cause coronary artery disease, stroke, and Moyamoya disease, along with thoracic aortic disease;Guo;Am. J. Hum. Genet,2009
4. Mutation of ACTA2 gene as an important cause of familial and nonfamilial nonsyndromatic thoracic aortic aneurysm and/or dissection (TAAD);Morisaki;Hum Mutat,2009
5. Aortic disease presentation and outcome associated with ACTA2 mutations;Regalado;Circ. Cardiovasc. Genet,2015
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