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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Pubblicato in:Stroke
Autori principali: 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.
Natura: Artigo
Lingua:Inglês
Pubblicazione: Lippincott Williams & Wilkins 2015
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Original Contributions
Accesso online: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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