Alexander disease
Definition:
References:
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[1]. Keiko Ishigaki, et al. TRH therapy in a patient with juvenile Alexander disease. Brain Dev. 2006 Nov;28(10):663-7. [Content Brief]
[2]. M Brenner, et al. Mutations in GFAP, encoding glial fibrillary acidic protein, are associated with Alexander disease. Nat Genet. 2001 Jan;27(1):117-20. [Content Brief]
[3]. Ming Der Perng, et al. The Alexander disease-causing glial fibrillary acidic protein mutant, R416W, accumulates into Rosenthal fibers by a pathway that involves filament aggregation and the association of alpha B-crystallin and HSP27. Am J Hum Genet. 2006 Aug;79(2):197-213. [Content Brief]
[4]. Rong Li, et al. GFAP mutations in Alexander disease. Int J Dev Neurosci. 2002 Jun-Aug;20(3-5):259-68. [Content Brief]
[5]. Roy A Quinlan, et al. GFAP and its role in Alexander disease. Exp Cell Res. 2007 Jun 10;313(10):2077-87. [Content Brief]
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