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

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

doi:10.1136/jnnp-2013-306116

Article info

PDF

PostScript

Letter

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

Authors

Jonathan D Rohrer Dementia Research Centre, Department of Neurodegenerative Disease, UCL Institute of Neurology, London, UK PubMed articles Google scholar articles
Jonathan Beck MRC Prion Unit, Department of Neurodegenerative Disease, UCL Institute of Neurology, London, UK PubMed articles Google scholar articles
Vincent Plagnol Department of Statistics, Institute of Genetics, University College London, UK PubMed articles Google scholar articles
Elizabeth Gordon Dementia Research Centre, Department of Neurodegenerative Disease, UCL Institute of Neurology, London, UK PubMed articles Google scholar articles
Tammaryn Lashley Queen Square Brain Bank, UCL Institute of Neurology, London, UK PubMed articles Google scholar articles
Tamas Revesz Queen Square Brain Bank, UCL Institute of Neurology, London, UK PubMed articles Google scholar articles
John C Janssen Department of Neurology, Chelsea and Westminster Hospital, London, UK PubMed articles Google scholar articles
Nick C Fox Dementia Research Centre, Department of Neurodegenerative Disease, UCL Institute of Neurology, London, UK PubMed articles Google scholar articles
Jason D Warren Dementia Research Centre, Department of Neurodegenerative Disease, UCL Institute of Neurology, London, UK PubMed articles Google scholar articles
Martin N Rossor Dementia Research Centre, Department of Neurodegenerative Disease, UCL Institute of Neurology, London, UK PubMed articles Google scholar articles
Simon Mead MRC Prion Unit, Department of Neurodegenerative Disease, UCL Institute of Neurology, London, UK PubMed articles Google scholar articles
Jonathan M Schott Dementia Research Centre, Department of Neurodegenerative Disease, UCL Institute of Neurology, London, UK PubMed articles Google scholar articles

Correspondence to Dr Jonathan M Schott, Institute of Neurology – Dementia Research Centre, Queen Square, London WC1N 3BG, UK; j.schott{at}ucl.ac.uk

View Full Text

Citation

Rohrer JD, Beck J, Plagnol V, et al

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

Journal of Neurology, Neurosurgery & Psychiatry 2013;84:1411-1412.

Publication history

First published July 31, 2013.

Online issue publication

April 13, 2016

Article Versions

Previous version (13 April 2016).
Previous version (13 April 2016).
You are viewing the most recent version of this article.

Request permissions

If you wish to reuse any or all of this article please use the link below which will take you to the Copyright Clearance Center’s RightsLink service. You will be able to get a quick price and instant permission to reuse the content in many different ways.

Copyright information

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/

Log in using your username and password

Main menu

Log in using your username and password

You are here

Authors

Citation

Publication history

Article Versions

Request permissions

Copyright information

Read the full text or download the PDF:

Log in using your username and password