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Prevalence and Atypical Clinical Characteristics of NOTCH3 Mutations Among Patients Admitted for Acute Lacunar Infarctions

Objectives: Cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy (CADASIL) is the most common hereditary small vessel disease, with reported frequencies of 2-5/100,000 individuals. Recently, it has been reported that some patients with NOTCH3 gene mutations show...

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Detalles Bibliográficos
Autores principales:	Okada, Takashi, Washida, Kazuo, Irie, Kenichi, Saito, Satoshi, Noguchi, Michio, Tomita, Tsutomu, Koga, Masatoshi, Toyoda, Kazunori, Okazaki, Shuhei, Koizumi, Takashi, Mizuta, Ikuko, Mizuno, Toshiki, Ihara, Masafumi
Formato:	Online Artículo Texto
Lenguaje:	English
Publicado:	Frontiers Media S.A. 2020
Materias:	Neuroscience
Acceso en línea:	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7240022/ https://www.ncbi.nlm.nih.gov/pubmed/32477100 http://dx.doi.org/10.3389/fnagi.2020.00130

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