Article (Scientific journals)
A distinct clinical phenotype in a German kindred with motor neuron disease carrying a CHCHD10 mutation.
Kurzwelly, Delia; Krüger, Stefanie; Biskup, Saskia et al.
2015In Brain: a Journal of Neurology, 138 (Pt 9), p. 376
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Keywords :
DNA, Mitochondrial; Mitochondrial Proteins; Amyotrophic Lateral Sclerosis/etiology; DNA, Mitochondrial/genetics; Female; Frontotemporal Dementia/etiology; Humans; Male; Mitochondria/pathology; Mitochondrial Diseases/complications; Mitochondrial Proteins/genetics; Amyotrophic Lateral Sclerosis; Frontotemporal Dementia; Mitochondria; Mitochondrial Diseases; Neurology (clinical)
Disciplines :
Neurology
Author, co-author :
Kurzwelly, Delia;  1 Department of Neurology, University of Bonn, Bonn, Germany 2 German Centre for Neurodegenerative Diseases (DZNE), Bonn, Germany
Krüger, Stefanie;  3 CeGaT GmbH - Centre for Genomics and Transcriptomics, Tübingen, Germany
Biskup, Saskia;  3 CeGaT GmbH - Centre for Genomics and Transcriptomics, Tübingen, Germany
HENEKA, Michael  ;  1 Department of Neurology, University of Bonn, Bonn, Germany 2 German Centre for Neurodegenerative Diseases (DZNE), Bonn, Germany michael.heneka@ukb.uni-bonn.de
External co-authors :
yes
Language :
English
Title :
A distinct clinical phenotype in a German kindred with motor neuron disease carrying a CHCHD10 mutation.
Publication date :
September 2015
Journal title :
Brain: a Journal of Neurology
ISSN :
0006-8950
eISSN :
1460-2156
Publisher :
Oxford University Press, England
Volume :
138
Issue :
Pt 9
Pages :
e376
Peer reviewed :
Peer Reviewed verified by ORBi
Available on ORBilu :
since 07 May 2024

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