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Novel mutation in MAPT exon 13 (p.N410H) causes corticobasal degeneration
In order to determine the frequency of microtubule associated protein tau gene (MAPT) mutations and rare variants in CBD, we performed a systematic sequence analysis of MAPT coding and 3′ untranslated region (3′UTR) in a large cohort of autopsy-confirmed CBD patients (N=109). This identified a novel...
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| Hauptverfasser: | , , , , , , , , , , , , , , , |
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| Format: | Artigo |
| Sprache: | Inglês |
| Veröffentlicht: |
2014
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| Schlagworte: | |
| Online Zugang: | https://ncbi.nlm.nih.gov/pmc/articles/PMC3943649/ https://ncbi.nlm.nih.gov/pubmed/24121548 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1007/s00401-013-1193-7 |
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