Cadasil - genetic and ultrastructural diagnosis: case report
ABSTRACT 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 mutation...
Furkejuvvon:
| Váldodahkkit: | , , , |
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| Materiálatiipa: | Artigo |
| Giella: | Inglês |
| Almmustuhtton: |
Academia Brasileira de Neurologia, Departamento de Neurologia Cognitiva e Envelhecimento
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| Ráidu: | Dementia & Neuropsychologia |
| Fáttát: | |
| Liŋkkat: | http://www.scielo.br/scielo.php?script=sci_arttext&pid=S1980-57642015000400428&lng=en&tlng=en |
| Fáddágilkorat: |
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