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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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| Pubblicato in: | Front Aging Neurosci |
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| Autori principali: | , , , , , , , , |
| Natura: | Artigo |
| Lingua: | Inglês |
| Pubblicazione: |
Frontiers Media S.A.
2016
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| Soggetti: | |
| Accesso online: | 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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