Loss-of-function mutations in RAB39B are associated with typical early-onset Parkinson disease. (June 2015)

Record Type:
Journal Article
Title:
Loss-of-function mutations in RAB39B are associated with typical early-onset Parkinson disease. (June 2015)
Main Title:
Loss-of-function mutations in RAB39B are associated with typical early-onset Parkinson disease
Authors:
Lesage, Suzanne
Bras, Jose
Cormier-Dequaire, Florence
Condroyer, Christel
Nicolas, Aude
Darwent, Lee
Guerreiro, Rita
Majounie, Elisa
Federoff, Monica
Heutink, Peter
Wood, Nicholas W.
Gasser, Thomas
Hardy, John
Tison, François
Singleton, Andrew
Brice, Alexis
Abstract:
Is Part Of:
Neurology. Volume 1:Number 1(2015)
Journal:
Neurology
Issue:
Volume 1:Number 1(2015)
Issue Display:
Volume 1, Issue 1 (2015)
Year:
2015
Volume:
1
Issue:
1
Issue Sort Value:
2015-0001-0001-0000
Page Start:
Page End:
Publication Date:
2015-06
Subjects:
Neurogenetics -- Periodicals
616.80442
Journal URLs:
http://ng.neurology.org/ ↗
http://journals.lww.com/pages/default.aspx ↗
DOI:
10.1212/NXG.0000000000000009 ↗
Languages:
English
ISSNs:
2376-7839
Deposit Type:
Legaldeposit
View Content:
Available online (eLD content is only available in our Reading Rooms) ↗
Physical Locations:
British Library DSC - BLDSS-3PM
British Library HMNTS - ELD Digital store
Ingest File:
6342.xml