Perng, M. D., Su, M., Wen, S. F., Li, R., Gibbon, T., Prescott, A. R., . . . Quinlan, R. A. (2006). 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. The American Society of Human Genetics.

Perng, Ming Der, Mu Su, Shu Fang Wen, Rong Li, Terry Gibbon, Alan R. Prescott, Michael Brenner, and Roy A. Quinlan. 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. The American Society of Human Genetics, 2006.

Perng, Ming Der, 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 αB-Crystallin and HSP27. The American Society of Human Genetics, 2006.