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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Detalles Bibliográficos
Autores principales: 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.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Lippincott Williams & Wilkins 2015
Materias:
Original Contributions
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4442025/
https://www.ncbi.nlm.nih.gov/pubmed/25953367
http://dx.doi.org/10.1161/STROKEAHA.114.008540

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4442025/
https://www.ncbi.nlm.nih.gov/pubmed/25953367
http://dx.doi.org/10.1161/STROKEAHA.114.008540

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