Article (Scientific journals)
MtDNA deletions discriminate affected from unaffected LRRK2 mutation carriers
Ouzren, Nassima; Delcambre, Sylvie; Ghelfi, Jenny et al.
2019In Annals of Neurology, 86 (2), p. 324-326
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Keywords :
Mitochondria; LRRK2-associated PD; mtDNA deletions
Disciplines :
Biochemistry, biophysics & molecular biology
Author, co-author :
Ouzren, Nassima ;  University of Luxembourg > Luxembourg Centre for Systems Biomedicine (LCSB)
Delcambre, Sylvie ;  University of Luxembourg > Luxembourg Centre for Systems Biomedicine (LCSB)
Ghelfi, Jenny ;  University of Luxembourg > Luxembourg Centre for Systems Biomedicine (LCSB)
Seibler, Philip;  University of Lübeck > Institute of Neurogenetics
Farrer, Matthew J.;  University of British Columbia - UBC > Department of Medical Genetics
König, Inke;  University of Lübeck > Institute of Medical Biometry and Statistics
Aasly, Jan O.;  St. Olav’s Hospital, Norwegian University of Science and Technology > Department of Neuromedicine and Movement Science and Department of Neurology
Trinh, Joanne;  University of Lübeck > Institute of Neurogenetics
Klein, Christine;  University of Lübeck > Institute of Neurogenetics
Grünewald, Anne  ;  University of Luxembourg > Luxembourg Centre for Systems Biomedicine (LCSB)
External co-authors :
yes
Language :
English
Title :
MtDNA deletions discriminate affected from unaffected LRRK2 mutation carriers
Publication date :
August 2019
Journal title :
Annals of Neurology
ISSN :
1531-8249
Publisher :
John Wiley & Sons, Hoboken, United States - New York
Volume :
86
Issue :
2
Pages :
324-326
Peer reviewed :
Peer Reviewed verified by ORBi
FnR Project :
FNR11250962 - Reduced Penetrance In Hereditary Movement Disorders: Elucidating Mechanisms Of Endogenous Disease Protection P1: Markers And Mechanisms Of Reduced Penetrance In Lrrk2 Mutation Carriers, 2016 (01/01/2017-30/06/2020) - Anne Grünewald
Funders :
FNR - Fonds National de la Recherche [LU]
DFG - Deutsche Forschungsgemeinschaft [DE]
Available on ORBilu :
since 25 July 2019

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