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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Bibliografske podrobnosti
izdano v:Front Aging Neurosci
Main Authors: Mizuno, Toshiki, Mizuta, Ikuko, Watanabe-Hosomi, Akiko, Mukai, Mao, Koizumi, Takashi
Format: Artigo
Jezik:Inglês
Izdano: Frontiers Media S.A. 2020
Teme:
Neuroscience
Online dostop:https://ncbi.nlm.nih.gov/pmc/articles/PMC7224236/
https://ncbi.nlm.nih.gov/pubmed/32457593
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.3389/fnagi.2020.00091
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