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A Japanese Case of CADASIL with a Rare Mutation in Exon 24 of the NOTCH3 Gene
A 50-year-old man with a family history of stroke and depression slowly developed brain lesions. Magnetic resonance imaging revealed hyperintense lesions in the diffuse white matter, external capsules, and temporal poles on T2-weighted imaging. A heterozygous mutation c.3879C＞G in exon 24 of the NOT...
Tallennettuna:
| Julkaisussa: | Intern Med |
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| Päätekijät: | , , , , , , |
| Aineistotyyppi: | Artigo |
| Kieli: | Inglês |
| Julkaistu: |
The Japanese Society of Internal Medicine
2018
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| Aiheet: | |
| Linkit: | https://ncbi.nlm.nih.gov/pmc/articles/PMC6232040/ https://ncbi.nlm.nih.gov/pubmed/29780132 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.2169/internalmedicine.0723-17 |
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