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

@article{Miyawaki2012IdentificationOA,
  title={Identification of a genetic variant common to moyamoya disease and intracranial major artery stenosis/occlusion.},
  author={Satoru Miyawaki and Hideaki Imai and Shunsaku Takayanagi and Akitake Mukasa and Hirofumi Nakatomi and Nobuhito Saito},
  journal={Stroke},
  year={2012},
  volume={43 12},
  pages={
          3371-4
        }
}
BACKGROUND AND PURPOSE The c.14576G>A variant in ring finger protein 213 (RNF213) was recently identified as a susceptibility gene variant for moyamoya disease (MMD). The occurrence of c.14576G>A variant was evaluated in patients with intracranial major artery stenosis/occlusion (ICASO) without signs of MMD (non-MMD ICASO), as well as in patients with MMD and other cerebrovascular diseases as controls. METHODS This single-hospital-based case-control study was completed in 7 months (from… CONTINUE READING

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