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A Novel Tau Mutation in Exon 12, p.Q336H, Causes Hereditary Pick Disease
Pick disease (PiD) is a frontotemporal lobar degeneration with distinctive neuronal inclusions (Pick bodies) that are enriched in 3-repeat (3R) tau. Although mostly sporadic, mutations in the tau gene (MAPT) have been reported. We screened 24 cases of neuropathologically confirmed PiD for MAPT mutat...
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| Gepubliceerd in: | J Neuropathol Exp Neurol |
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| Hoofdauteurs: | , , , , , , , , , , |
| Formaat: | Artigo |
| Taal: | Inglês |
| Gepubliceerd in: |
2015
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| Onderwerpen: | |
| Online toegang: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4607649/ https://ncbi.nlm.nih.gov/pubmed/26426266 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1097/NEN.0000000000000248 |
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