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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Detalles Bibliográficos
Autores principales: Ishii, Kazuhiro, Tozaka, Naoki, Tsutsumi, Satoshi, Muroi, Ai, Tamaoka, Akira
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Wolters Kluwer Health 2020
Materias:
5300
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7373609/
https://www.ncbi.nlm.nih.gov/pubmed/32702807
http://dx.doi.org/10.1097/MD.0000000000019800

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7373609/
https://www.ncbi.nlm.nih.gov/pubmed/32702807
http://dx.doi.org/10.1097/MD.0000000000019800

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