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Type II (adult onset) Alexander disease in a paraplegic male with a rare D128N mutation in the GFAP gene

Abstract not available.

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Foilsithe in:Clin Neuropathol
Main Authors: Chang, Ki-Eun, Pratt, Drew, Mishra, Bibhuti B., Edwards, Nancy, Hallett, Mark, Ray-Chaudhury, Abhik
Formáid: Artigo
Teanga:Inglês
Foilsithe: Dustri-Verlag Dr. Karl Feistle 2015
Ábhair:
Rochtain Ar Líne:https://ncbi.nlm.nih.gov/pmc/articles/PMC4766795/
https://ncbi.nlm.nih.gov/pubmed/25997626
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.5414/NP300863
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