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Article

RNF213 p.R4810K Polymorphism and the Risk of Moyamoya Disease, Intracranial Major Artery Stenosis/Occlusion, and Quasi-Moyamoya Disease: A Meta-Analysis.

Journal of stroke and cerebrovascular diseases : the official journal of National Stroke Association - 1 Aug 2018

Wang Yue, Mambiya Michael, Li Qian, Yang Luping, Jia He, Han Yibo, Liu Wanyang

Abstract excerpt

BACKGROUND: Accumulating studies have reported that there is an association between the Ring finger protein 213 (RNF213) p.R4810K (rs112735431, c.14576G>A) single nucleotide polymorphism and the predisposition of moyamoya disease (MMD), intracranial major artery stenosis/occlusion (ICASO), quasi-moyamoya disease (quasi-MMD), and other vascular diseases. However, to this day, analyses about this association have...

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Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Adenosine Triphosphatases
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Share to Constriction, Pathologic
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Share to Polymorphism, Single Nucleotide
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Source

Identifiers

PMID: 29752070
DOI: 10.1016/j.jstrokecerebrovasdis.2018.04.013

Genes

MMD

Variants

rs112735431

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-07.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

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RNF213 p.R4810K Polymorphism and the Risk of Moyamoya Disease, Intracranial Major Artery Stenosis/Occlusion, and Quasi-Moyamoya Disease: A Meta-Analysis.PMID 29752070Read ↗

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