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Brain. 2014 Dec;137(Pt 12):e309. doi: 10.1093/brain/awu227. Epub 2014 Aug 11.

Two novel mutations in conserved codons indicate that CHCHD10 is a gene associated with motor neuron disease.

Author information

1
1 Department of Neurology, Ulm University, Ulm, Germany.
2
1 Department of Neurology, Ulm University, Ulm, Germany 2 Department of Pharmacology and Clinical Neuroscience, Umeå University, Umeå, Sweden 3 Virtual Helmholtz Institute RNA Dysmetabolism in Amyotrophic Lateral Sclerosis and Fronto-Temporal Dementia, Germany.
3
1 Department of Neurology, Ulm University, Ulm, Germany 4 Institute of Human Genetics, Ulm University, Ulm, Germany.
4
4 Institute of Human Genetics, Ulm University, Ulm, Germany.
5
5 Institute of Human Genetics, Helmholtz Zentrum München, Neuherberg, Germany, and Insitute of Human Genetics, Technische Universität München, Munich, Germany.
6
1 Department of Neurology, Ulm University, Ulm, Germany 3 Virtual Helmholtz Institute RNA Dysmetabolism in Amyotrophic Lateral Sclerosis and Fronto-Temporal Dementia, Germany.
7
1 Department of Neurology, Ulm University, Ulm, Germany jochen.weishaupt@uni-ulm.de.
PMID:
25113787
DOI:
10.1093/brain/awu227
[Indexed for MEDLINE]

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