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GFAP Mutation in Alexander's Disease

The cause of Alexander's disease, a very rare, inherited CNS disorder, has been traced to the gene for glial fibrillary acidic protein (GFAP), according to a report published in this month's Nature Genetics...

Society for Neuroscience (SfN) Annual Meeting 2000

Society for Neuroscience Annual Meeting: Role of Nicastrin-Presenilin Complexes Society for Neuroscience Annual Meeting: Chromosome Missegregation Linked to PS Mutations Society for Neuroscience Annual Meeting: Presenilin and COX-2 Expression Induced by ...

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