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 αB-Crystallin and HSP27-Reference-Cited by-同舟云学术

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 αB-Crystallin and HSP27

Published:2006-08 Issue:2 Volume:79 Page:197-213
ISSN:0002-9297
Container-title:The American Journal of Human Genetics
language:en
Short-container-title:The American Journal of Human Genetics

Author:

Perng Ming Der,Su Mu,Wen Shu Fang,Li Rong,Gibbon Terry,Prescott Alan R.,Brenner Michael,Quinlan Roy A.

Publisher

Elsevier BV

Subject

Genetics(clinical),Genetics

Reference64 articles.

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4. Infantile and juvenile presentations of Alexander’s disease: a report of two cases;Deprez;Acta Neurol Scand,1999

5. Infantile Alexander disease: spectrum of GFAP mutations and genotype-phenotype correlation;Rodriguez;Am J Hum Genet,2001

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