CCM2 expression parallels that of CCM1.

Abstract

BACKGROUND AND PURPOSE Mutations in CCM2 (MGC4607 or malcavernin) cause familial cerebral cavernous malformation (CCM), an autosomal dominant neurovascular disease. Both the function of this molecule and the pathogenesis of the disease remain elusive. METHODS We analyzed the mRNA expression of Ccm1 and Ccm2 in the embryonic and postnatal mouse brain by in… (More)

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Cite this paper

@article{eker2006CCM2EP, title={CCM2 expression parallels that of CCM1.}, author={Aşkin Şeker and Katie L Pricola and Bulent Guclu and Ali K. Ozturk and Angeliki Louvi and Murat Gunel}, journal={Stroke}, year={2006}, volume={37 2}, pages={518-23} }