A novel CCM2 gene mutation associated with family cerebral cavernous malformation

A novel CCM2 gene mutation associated with family 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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Bibliographic Details
Main Authors: Wen-Qing Huang, Cong-Xia Lu, Ya Zhang, Ke-Hui Yi, Liang-Liang Cai, Ming-Li Li, Han Wang, Qing Lin, Chi-Meng Tzeng
Format: Article
Language:English
Published: Frontiers Media S.A. 2016-09-01
Series:Frontiers in Aging Neuroscience
Subjects:
Mutation
biomarker
Pathogenesis
CCM2
Susceptibility-weighted imaging (SWI)
Familial cerebral cavernous malformations (FCCM)
Online Access:http://journal.frontiersin.org/Journal/10.3389/fnagi.2016.00220/full

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http://journal.frontiersin.org/Journal/10.3389/fnagi.2016.00220/full

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