Please use this identifier to cite or link to this item: http://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/
RMID: 0030128219
DOI: 10.1136/jnnp-2013-306116
Appears in Collections:Medicine publications

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