Significant Association of the RNF213 p.R4810K Polymorphism with Quasi-Moyamoya Disease

Author:

Morimoto Takaaki,Mineharu YoheiORCID,Kobayashi HatasuORCID,Harada Kouji H.,Funaki Takeshi,Takagi Yasushi,Sakai Nobuyuki,Miyamoto Susumu,Koizumi Akio

Publisher

Elsevier BV

Subject

Cardiology and Cardiovascular Medicine,Clinical Neurology,Rehabilitation,Surgery

Reference23 articles.

1. Moyamoya disease and moyamoya syndrome;Scott;N Engl J Med,2009

2. A genome-wide association study identifies RNF213 as the first Moyamoya disease gene;Kamada;J Hum Genet,2011

3. Identification of RNF213 as a susceptibility gene for moyamoya disease and its possible role in vascular development;Liu;PLoS ONE,2011

4. Genetic variant RNF213 c.14576G>A in various phenotypes of intracranial major artery stenosis/occlusion;Miyawaki;Stroke,2013

5. Guidelines for diagnosis and treatment of moyamoya disease (spontaneous occlusion of the circle of Willis);Research Committee on the Pathology and Treatment of Spontaneous Occlusion of the Circle of Willis; Health Labour Sciences Research Grant for Research on Measures for Intractable Diseases;Neurol Med Chir (Tokyo),2012

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