Novel KRIT1 Mutation and No Molecular Evidence of Anticipation in a Family with Cerebral and Spinal Cavernous Malformations

Publisher： Karger

E-ISSN： 1421-9913|61|3|154-158

ISSN： 0014-3022

Source： European Neurology, Vol.61, Iss.3, 2008-12, pp. : 154-158

Disclaimer: Any content in publications that violate the sovereignty, the constitution or regulations of the PRC is not accepted or approved by CNPIEC.

Previous Menu Next

Abstract

Related content

Cerebral Cavernous Malformations and Unilateral Moyamoya in a Patient with a New Mutation in the KRIT-1/CCM1 Gene

By  

Cerebrovascular Diseases, Vol. 38, Iss. 4, 2014-11 ,pp. : 311-312

Karger

Access to resources Recommend Favorite

Cerebral Cavernous Malformation: A Portuguese Family with a Novel CCM1 Mutation

By  

Case Reports in Neurology, Vol. 8, Iss. 3, 2016-09 ,pp. : 193-198

Karger

Access to resources Recommend Favorite

Association of Cardiovascular Risk Factors with Disease Severity in Cerebral Cavernous Malformation Type 1 Subjects with the Common Hispanic Mutation

By  

Cerebrovascular Diseases, Vol. 37, Iss. 1, 2013-12 ,pp. : 57-63

Karger

Access to resources Recommend Favorite

Thoracic Intra- and Extramedullary Cavernous Hemangioma Associated with Innumerable Cerebral Vascular Malformations: Case Report and Review of the Literature

By  

Cerebrovascular Diseases, Vol. 16, Iss. 3, 2003-07 ,pp. : 297-301

Karger

Access to resources Recommend Favorite

Identification and Molecular Characterization of a Novel Splice-Site Mutation ( G1205C ) in the SQSTM1 Gene Causing Paget’s Disease of Bone in an Extended American Family

By Beyens G.   Wuyts W.   Cleiren E.   Freitas F.   Tiegs R.   Hul W.  

Calcified Tissue International, Vol. 79, Iss. 5, 2006-11 ,pp. : 281-288

Springer Publishing Company

Access to resources Recommend Favorite