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Article

Genetic variant RNF213 c.14576G>A in various phenotypes of intracranial major artery stenosis/occlusion.

Stroke - 1 Oct 2013

Miyawaki Satoru, Imai Hideaki, Shimizu Masahiro, Yagi Shinichi, Ono Hideaki, Mukasa Akitake, Nakatomi Hirofumi, Shimizu Tsuneo, Saito Nobuhito

Abstract excerpt

BACKGROUND AND PURPOSE: Recently, we reported a common genetic variant, ring finger protein 213 (RNF213) c.14576G>A variant, a susceptibility gene for moyamoya disease (MMD), among patients with intracranial major artery stenosis/occlusion (ICASO) in a selected Japanese population. The aim of this 2-center-based case-control study was to confirm our previous finding in a larger population. METHODS: Study...

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Identifiers

PMID: 23970789
DOI: 10.1161/STROKEAHA.113.002477

Genes

MMD

Variants

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Genetic variant RNF213 c.14576G>A in various phenotypes of intracranial major artery stenosis/occlusion.PMID 23970789Read ↗

Identification of a genetic variant common to moyamoya disease and intracranial major artery stenosis/occlusion.Semantic proximity Read ↗

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Genetic Analysis of Ring Finger Protein 213 (RNF213) c.14576G>A in Intracranial Atherosclerosis of the Anterior and Posterior Circulations.Semantic proximity Read ↗

Genetic Analysis of RNF213 c.14576G>A Variant in Nonatherosclerotic Quasi-Moyamoya Disease.Semantic proximity Read ↗

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A Polymorphism in RNF213 Is a Susceptibility Gene for Intracranial Atherosclerosis.Semantic proximity Read ↗

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