Adelaide Research & Scholarship
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https://hdl.handle.net/2440/121838
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| Type: | Journal article |
| Title: | Exome sequencing reveals a novel partial deletion in the progranulin gene causing primary progressive aphasia |
| Author: | Rohrer, J.D. Beck, J. Plagnol, V. Gordon, E. Lashley, T. Revesz, T. Janssen, J.C. Fox, N.C. Warren, J.D. Rossor, M.N. Mead, S. Schott, J.M. |
| Citation: | Journal of Neurology, Neurosurgery and Psychiatry, 2013; 84(12):1411-+ |
| Publisher: | BMJ Publishing Group |
| Issue Date: | 2013 |
| ISSN: | 0022-3050 1468-330X |
| Statement of Responsibility: | Jonathan D Rohrer, Jonathan Beck, Vincent Plagnol, Elizabeth Gordon, Tammaryn Lashley, Tamas Revesz, John C Janssen, Nick C Fox, Jason D Warren, Martin N Rossor, Simon Mead, Jonathan M Schott |
| Abstract: | Abstract not available |
| Keywords: | Humans Aphasia, Primary Progressive Genetic Predisposition to Disease Intercellular Signaling Peptides and Proteins Gene Deletion Male Exome Progranulins |
| Rights: | 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/ |
| DOI: | 10.1136/jnnp-2013-306116 |
| Published version: | http://dx.doi.org/10.1136/jnnp-2013-306116 |
| Appears in Collections: | Aurora harvest 8 Medicine publications |
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