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Exome sequencing reveals a novel partial deletion in the progranulin gene causing primary progressive aphasia
Autores principales: | , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BMJ Publishing Group
2013
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3905627/ https://www.ncbi.nlm.nih.gov/pubmed/23904625 http://dx.doi.org/10.1136/jnnp-2013-306116 |
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author | Rohrer, Jonathan D Beck, Jonathan Plagnol, Vincent Gordon, Elizabeth Lashley, Tammaryn Revesz, Tamas Janssen, John C Fox, Nick C Warren, Jason D Rossor, Martin N Mead, Simon Schott, Jonathan M |
author_facet | Rohrer, Jonathan D Beck, Jonathan Plagnol, Vincent Gordon, Elizabeth Lashley, Tammaryn Revesz, Tamas Janssen, John C Fox, Nick C Warren, Jason D Rossor, Martin N Mead, Simon Schott, Jonathan M |
author_sort | Rohrer, Jonathan D |
collection | PubMed |
description | |
format | Online Article Text |
id | pubmed-3905627 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2013 |
publisher | BMJ Publishing Group |
record_format | MEDLINE/PubMed |
spelling | pubmed-39056272014-01-29 Exome sequencing reveals a novel partial deletion in the progranulin gene causing primary progressive aphasia Rohrer, Jonathan D Beck, Jonathan Plagnol, Vincent Gordon, Elizabeth Lashley, Tammaryn Revesz, Tamas Janssen, John C Fox, Nick C Warren, Jason D Rossor, Martin N Mead, Simon Schott, Jonathan M J Neurol Neurosurg Psychiatry PostScript BMJ Publishing Group 2013-12 2013-07-31 /pmc/articles/PMC3905627/ /pubmed/23904625 http://dx.doi.org/10.1136/jnnp-2013-306116 Text en Published by the BMJ Publishing Group Limited. For permission to use (where not already granted under a licence) please go to http://group.bmj.com/group/rights-licensing/permissions This is an Open Access article distributed in accordance with the terms of the Creative Commons Attribution (CC BY 3.0) license, which permits others to distribute, remix, adapt and build upon this work, for commercial use, provided the original work is properly cited. See: http://creativecommons.org/licenses/by/3.0/ |
spellingShingle | PostScript Rohrer, Jonathan D Beck, Jonathan Plagnol, Vincent Gordon, Elizabeth Lashley, Tammaryn Revesz, Tamas Janssen, John C Fox, Nick C Warren, Jason D Rossor, Martin N Mead, Simon Schott, Jonathan M Exome sequencing reveals a novel partial deletion in the progranulin gene causing primary progressive aphasia |
title | Exome sequencing reveals a novel partial deletion in the progranulin gene causing primary progressive aphasia |
title_full | Exome sequencing reveals a novel partial deletion in the progranulin gene causing primary progressive aphasia |
title_fullStr | Exome sequencing reveals a novel partial deletion in the progranulin gene causing primary progressive aphasia |
title_full_unstemmed | Exome sequencing reveals a novel partial deletion in the progranulin gene causing primary progressive aphasia |
title_short | Exome sequencing reveals a novel partial deletion in the progranulin gene causing primary progressive aphasia |
title_sort | exome sequencing reveals a novel partial deletion in the progranulin gene causing primary progressive aphasia |
topic | PostScript |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3905627/ https://www.ncbi.nlm.nih.gov/pubmed/23904625 http://dx.doi.org/10.1136/jnnp-2013-306116 |
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