Clinical and Genetic Aspects of CADASIL

Cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy (CADASIL), a hereditary cerebral small vessel disease caused by mutations in NOTCH3, is characterized by recurrent stroke without vascular risk factors, mood disturbances, and dementia. MRI imaging shows cereb...

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Detalles Bibliográficos
Autores principales: Mizuno, Toshiki, Mizuta, Ikuko, Watanabe-Hosomi, Akiko, Mukai, Mao, Koizumi, Takashi
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/PMC7224236/
https://www.ncbi.nlm.nih.gov/pubmed/32457593
http://dx.doi.org/10.3389/fnagi.2020.00091

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7224236/
https://www.ncbi.nlm.nih.gov/pubmed/32457593
http://dx.doi.org/10.3389/fnagi.2020.00091

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