Cadasil – genetic and ultrastructural diagnosis. Case report
Cerebral Autosomal Dominant Arteriopathy with Subcortical Infarcts and Leukoencephalopathy (CADASIL) is a hereditary disorder which affects the cerebral vasculature due to mutations in the NOTCH 3 gene. The diagnosis may be established through genetic testing for detection of these mutations and/or...
Furkejuvvon:
| Publikašuvnnas: | Dementia & Neuropsychologia |
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| Váldodahkkit: | , , , |
| Materiálatiipa: | Artigo |
| Giella: | Inglês |
| Almmustuhtton: |
Associação Neurologia Cognitiva e do Comportamento
2015
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| Fáttát: | |
| Liŋkkat: | https://www.redalyc.org/articulo.oa?id=339543263016 |
| Fáddágilkorat: |
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