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Familial cerebral cavernous malformation presenting with epilepsy caused by mutation in the CCM2 gene: A case report
RATIONALE: Cerebral cavernous malformation (CCM) of the familial type is caused by abnormalities in the CCM1, CCM2, and CCM3 genes. These 3 proteins forming a complex associate with the maintenance of vascular endothelial cell-cell junctions. Dysfunction of these proteins results in the development...
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| Publicado no: | Medicine (Baltimore) |
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| Main Authors: | , , , , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
Wolters Kluwer Health
2020
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC7373609/ https://ncbi.nlm.nih.gov/pubmed/32702807 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1097/MD.0000000000019800 |
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