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Cerebral small vessel disease due to a unique heterozygous HTRA1 mutation in an African man
OBJECTIVE: To describe the case of an African patient who was diagnosed with cerebral autosomal recessive arteriopathy with subcortical infarcts and leukoencephalopathy (CARASIL). METHODS: Case report and literature review. RESULTS: We present a 39-year-old Gabonese man who developed progressive gai...
Tallennettuna:
| Julkaisussa: | Neurol Genet |
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| Päätekijät: | , , , , , , |
| Aineistotyyppi: | Artigo |
| Kieli: | Inglês |
| Julkaistu: |
Wolters Kluwer
2019
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| Aiheet: | |
| Linkit: | https://ncbi.nlm.nih.gov/pmc/articles/PMC6936311/ https://ncbi.nlm.nih.gov/pubmed/32042911 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1212/NXG.0000000000000382 |
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