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Systematic Validation of RNF213 Coding Variants in Japanese Patients With Moyamoya Disease
BACKGROUND: A founder variant of RNF213, p.R4810K (c.14429G>A, rs112735431), was recently identified as a major genetic risk factor for moyamoya disease (MMD) in Japan. Although the association of p.R4810K was reported to be highly significant and reproducible, the disease susceptibility of other...
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| 出版年: | J Am Heart Assoc |
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| 主要な著者: | , , , , , , , , , |
| フォーマット: | Artigo |
| 言語: | Inglês |
| 出版事項: |
John Wiley & Sons, Ltd
2015
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| 主題: | |
| オンライン･アクセス: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4599414/ https://ncbi.nlm.nih.gov/pubmed/25964206 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1161/JAHA.115.001862 |
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