ACTA2 is not a Major Genetic Risk Gene for Chinese Patients with Moyamoya Disease
Author:
Affiliation:
1. Department of Neurology, West China Hospital, Sichuan University, Chengdu, China
2. Department of Neurology, Renmin Hospital, Hubei University of Medicine, Shiyan, China
Publisher
SAGE Publications
Subject
Neurology
Link
http://journals.sagepub.com/doi/pdf/10.1111/ijs.12074
Reference3 articles.
1. Mutations in Smooth Muscle Alpha-Actin (ACTA2) Cause Coronary Artery Disease, Stroke, and Moyamoya Disease, Along with Thoracic Aortic Disease
2. ACTA2 is not a major disease-causing gene for moyamoya disease
3. Analysis of ACTA2 in European Moyamoya disease patients
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3. ACTA2 Cerebral Arteriopathy: Not Just a Puff of Smoke;Cerebrovascular Diseases;2018
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5. Indirect and direct revascularization of ACTA2 cerebral arteriopathy: feasibility of the superficial temporal artery to anterior cerebral artery bypass with posterior auricular artery interposition graft: case report;Journal of Neurosurgery: Pediatrics;2016-09
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