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A Novel CCM2 Gene Mutation Associated with Familial Cerebral Cavernous Malformation
Background: Cerebral cavernous malformations (CCMs) are common vascular malformations that predominantly arise in the central nervous system and are mainly characterized by enlarged vascular cavities without intervening brain parenchyma. Familial CCMs (FCCMs) is inherited in an autosomal dominant pa...
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| Publicat a: | Front Aging Neurosci |
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| Autors principals: | , , , , , , , , |
| Format: | Artigo |
| Idioma: | Inglês |
| Publicat: |
Frontiers Media S.A.
2016
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| Matèries: | |
| Accés en línia: | https://ncbi.nlm.nih.gov/pmc/articles/PMC5030299/ https://ncbi.nlm.nih.gov/pubmed/27708576 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.3389/fnagi.2016.00220 |
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