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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Detalles Bibliográficos
Autores principales: Huang, Wen-Qing, Lu, Cong-Xia, Zhang, Ya, Yi, Ke-Hui, Cai, Liang-Liang, Li, Ming-Li, Wang, Han, Lin, Qing, Tzeng, Chi-Meng
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2016
Materias:
Neuroscience
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5030299/
https://www.ncbi.nlm.nih.gov/pubmed/27708576
http://dx.doi.org/10.3389/fnagi.2016.00220

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5030299/
https://www.ncbi.nlm.nih.gov/pubmed/27708576
http://dx.doi.org/10.3389/fnagi.2016.00220

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