Common NOTCH3 Variants and Cerebral Small-Vessel Disease

BACKGROUND AND PURPOSE—: The most common monogenic cause of cerebral small-vessel disease is cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy, caused by NOTCH3 gene mutations. It has been hypothesized that more common variants in NOTCH3 may also contribute t...

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書誌詳細
出版年:Stroke
主要な著者: Rutten-Jacobs, Loes C.A., Traylor, Matthew, Adib-Samii, Poneh, Thijs, Vincent, Sudlow, Cathie, Rothwell, Peter M., Boncoraglio, Giorgio, Dichgans, Martin, Bevan, Steve, Meschia, James, Levi, Christopher, Rost, Natalia S., Rosand, Jonathan, Hassan, Ahamad, Markus, Hugh S.
フォーマット: Artigo
言語:Inglês
出版事項: Lippincott Williams & Wilkins 2015
主題:
Original Contributions
オンライン･アクセス:https://ncbi.nlm.nih.gov/pmc/articles/PMC4442025/
https://ncbi.nlm.nih.gov/pubmed/25953367
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1161/STROKEAHA.114.008540
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