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Department of Neuroscience, Mayo Clinic | 論文
- Heterogeneous inclusions in neurofilament inclusion disease
- A presenilin 1 mutation (L420R) in a family with early onset Alzheimer disease, seizures and cotton wool plaques, but not spastic paraparesis
- Commentary on Functional analysis of APOE Locus genetic variation implicates regional enhancers in the regulation of both TOMM40 and APOE