Article
A novel GFAP mutation and disseminated white matter lesions: adult Alexander disease?
European neurology - 1 Jan 2003
Brockmann Knut, Meins Moritz, Taubert Angelika, Trappe Ralf, Grond Martin, Hanefeld Folker
Abstract excerpt
The recent discovery of heterozygous de novo mutations in the glial fibrillary acidic protein (GFAP) gene as the cause of infantile and juvenile Alexander disease has shed new light on the long-standing debate whether the adult subtype has the same etiology as infantile and juvenile Alexander dis...
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