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de novo MAPT mutation G335A causes severe brain atrophy, 3R and 4R PHF-tau pathology and early onset frontotemporal dementia
Autores principales: | , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7325098/ https://www.ncbi.nlm.nih.gov/pubmed/32600421 http://dx.doi.org/10.1186/s40478-020-00977-8 |
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author | Ando, Kunie Ferlini, Lorenzo Suain, Valérie Yilmaz, Zehra Mansour, Salwa Le Ber, Isabelle Bouchard, Cécile Leroy, Karelle Durr, Alexandra Clot, Fabienne Sarazin, Marie Bier, Jean-Christophe Brion, Jean-Pierre |
author_facet | Ando, Kunie Ferlini, Lorenzo Suain, Valérie Yilmaz, Zehra Mansour, Salwa Le Ber, Isabelle Bouchard, Cécile Leroy, Karelle Durr, Alexandra Clot, Fabienne Sarazin, Marie Bier, Jean-Christophe Brion, Jean-Pierre |
author_sort | Ando, Kunie |
collection | PubMed |
description | |
format | Online Article Text |
id | pubmed-7325098 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-73250982020-06-30 de novo MAPT mutation G335A causes severe brain atrophy, 3R and 4R PHF-tau pathology and early onset frontotemporal dementia Ando, Kunie Ferlini, Lorenzo Suain, Valérie Yilmaz, Zehra Mansour, Salwa Le Ber, Isabelle Bouchard, Cécile Leroy, Karelle Durr, Alexandra Clot, Fabienne Sarazin, Marie Bier, Jean-Christophe Brion, Jean-Pierre Acta Neuropathol Commun Letter to the Editor BioMed Central 2020-06-29 /pmc/articles/PMC7325098/ /pubmed/32600421 http://dx.doi.org/10.1186/s40478-020-00977-8 Text en © The Author(s) 2020 Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated in a credit line to the data. |
spellingShingle | Letter to the Editor Ando, Kunie Ferlini, Lorenzo Suain, Valérie Yilmaz, Zehra Mansour, Salwa Le Ber, Isabelle Bouchard, Cécile Leroy, Karelle Durr, Alexandra Clot, Fabienne Sarazin, Marie Bier, Jean-Christophe Brion, Jean-Pierre de novo MAPT mutation G335A causes severe brain atrophy, 3R and 4R PHF-tau pathology and early onset frontotemporal dementia |
title | de novo MAPT mutation G335A causes severe brain atrophy, 3R and 4R PHF-tau pathology and early onset frontotemporal dementia |
title_full | de novo MAPT mutation G335A causes severe brain atrophy, 3R and 4R PHF-tau pathology and early onset frontotemporal dementia |
title_fullStr | de novo MAPT mutation G335A causes severe brain atrophy, 3R and 4R PHF-tau pathology and early onset frontotemporal dementia |
title_full_unstemmed | de novo MAPT mutation G335A causes severe brain atrophy, 3R and 4R PHF-tau pathology and early onset frontotemporal dementia |
title_short | de novo MAPT mutation G335A causes severe brain atrophy, 3R and 4R PHF-tau pathology and early onset frontotemporal dementia |
title_sort | de novo mapt mutation g335a causes severe brain atrophy, 3r and 4r phf-tau pathology and early onset frontotemporal dementia |
topic | Letter to the Editor |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7325098/ https://www.ncbi.nlm.nih.gov/pubmed/32600421 http://dx.doi.org/10.1186/s40478-020-00977-8 |
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