Intracranial vessel stenosis in a young patient with an MYH11 mutation: A case report and review of two prior cases.
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DOI: 10.1016/j.wneu.2020.02.054
Abstract: BACKGROUND The MYH11 gene codes for smooth muscle myosin heavy chain which has a critical function in maintaining vascular wall stability. Patients with this mutation most commonly have aortic and cardiac defects. Documented involvement of… read more here.
Keywords: myh11; stenosis young; stenosis; intracranial vessel ... See more keywords