An infantile case of Alexander disease unusual for its MRI features and a GFAP allele carrying both the p.Arg79His mutation and the p.Glu223Gln coding variant

An infantile case of Alexander disease unusual for its MRI features and a GFAP allele carrying both the p.Arg79His mutation and the p.Glu223Gln coding variant

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Bibliographic Details
Published in:Journal of neurology Vol. 256; no. 4; pp. 679 - 682
Main Authors: Dotti, Maria Teresa, Buccoliero, Rosaria, Lee, Andrew, Gorospe, J Raphael, Flint, Daniel, Galluzzi, Paolo, Bianchi, Silvia, D'Eramo, Camilla, Naidu, Sakkubai, Federico, Antonio, Brenner, Michael
Format: Report
Language:English
Published: 01-04-2009
Online Access:Get full text
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Description
Bibliography:ObjectType-Article-2
ObjectType-Correspondence-1
ObjectType-Case Study-4
content type line 59
SourceType-Reports-1
ObjectType-Report-3
ISSN:1432-1459
DOI:10.1007/s00415-009-0147-4