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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Detalhes bibliográficos
Publicado no:Front Aging Neurosci
Main Authors: 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: Artigo
Idioma:Inglês
Publicado em: Frontiers Media S.A. 2016
Assuntos:
Neuroscience
Acesso em linha: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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