Differences in the Genotype Frequency of the RNF213 Variant in Patients with Familial Moyamoya Disease in Kyushu, Japan

The p.R4810K (rs11273543, c.14429G > A) variant of the RNF213 gene is associated with increased risk of Moyamoya disease (MMD), which is an idiopathic progressive intracranial vascular steno-occlusive disease, in Asian populations. Numerous variant association studies for this MMD variant have be...

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Detalles Bibliográficos
Autores principales: TAKAMATSU, Yuichiro, HIGASHIMOTO, Ken, MAEDA, Toshiyuki, KAWASHIMA, Masatou, MATSUO, Muneaki, ABE, Tatsuya, MATSUSHIMA, Toshio, SOEJIMA, Hidenobu
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Japan Neurosurgical Society 2017
Materias:
Original Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5709714/
https://www.ncbi.nlm.nih.gov/pubmed/28931766
http://dx.doi.org/10.2176/nmc.oa.2017-0036

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5709714/
https://www.ncbi.nlm.nih.gov/pubmed/28931766
http://dx.doi.org/10.2176/nmc.oa.2017-0036

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