دورية أكاديمية

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

التفاصيل البيبلوغرافية
العنوان: 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
المؤلفون: 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
المصدر: Journal of Neurology. April 2009 256(4):679-682
قاعدة البيانات: Springer Nature Journals
الوصف
تدمد:03405354
14321459
DOI:10.1007/s00415-009-0147-4