Three novel mutations in the ACTA2 gene in German patients with thoracic aortic aneurysms and dissections

Genetic Analysis of Young Adult Patients With Aortic Disease Not Fulfilling the Diagnostic Criteria for Marfan Syndrome

(2010) Koichi Akutsu et al.   CIRCULATION JOURNAL

Cap myopathy caused by a mutation of the skeletal alpha-actin gene ACTA1

(2010) Ryan M. Hung et al.   NEUROMUSCULAR DISORDERS

Mutations in Smooth Muscle Alpha-Actin (ACTA2) Cause Coronary Artery Disease, Stroke, and Moyamoya Disease, Along with Thoracic Aortic Disease

(2009) Dong-Chuan Guo et al.   AMERICAN JOURNAL OF HUMAN GENETICS

Mutations and polymorphisms of the skeletal muscle α-actin gene (ACTA1)

(2009) Nigel G. Laing et al.   HUMAN MUTATION

Mutation ofACTA2gene as an important cause of familial and nonfamilial nonsyndromatic thoracic aortic aneurysm and/or dissection (TAAD)

(2009) Hiroko Morisaki et al.   HUMAN MUTATION

The nature of the globular- to fibrous-actin transition

(2009) Toshiro Oda et al.   NATURE

Genetic Basis of Thoracic Aortic Aneurysms and Dissections: Focus on Smooth Muscle Cell Contractile Dysfunction

(2008) Dianna M. Milewicz et al.   Annual Review of Genomics and Human Genetics