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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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| Publicat a: | Front Aging Neurosci |
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| Autors principals: | , , , , |
| Format: | Artigo |
| Idioma: | Inglês |
| Publicat: |
Frontiers Media S.A.
2020
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| Matèries: | |
| Accés en línia: | 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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