Á lódáil...
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 |
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Main Authors: | , , , , , |
Formáid: | Artigo |
Teanga: | Inglês |
Foilsithe: |
Dustri-Verlag Dr. Karl Feistle
2015
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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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