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Exome sequencing reveals a novel partial deletion in the progranulin gene causing primary progressive aphasia

Detalles Bibliográficos
Autores principales: 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
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BMJ Publishing Group 2013
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
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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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