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Brain. 2014 Dec;137(Pt 12):e311. doi: 10.1093/brain/awu265. Epub 2014 Sep 26.

Mutations in the CHCHD10 gene are a common cause of familial amyotrophic lateral sclerosis.

Author information

1
1 Neuromuscular Diseases Research Section, Laboratory of Neurogenetics, National Institute on Aging, Bethesda, MD 20892, USA.
2
2 Computational Biology Core, Laboratory of Neurogenetics, National Institute on Aging, Bethesda, MD 20892, USA.
3
3 Molecular Genetics Section, Laboratory of Neurogenetics, National Institute on Aging, Bethesda, MD 20892, USA.
4
4 Neurological Institute, Catholic University and Insieme Contro le Malattie del Motoneurone Association for ALS Research, Largo Agostino Gemelli 8, Rome 00168, Italy.
5
5 Molecular Genetics Unit, Department of Clinical Pathology, Azienda Sanitaria Ospedaliera Ospedale Infantile Regina Margherita-Santa Anna, Turin 10126, Italy.
6
6 Department of Neurology, Sourasky Medical Centre, 6 Weizmann Street, Tel Aviv 64239, Israel.
7
7 'Rita Levi Montalcini' Department of Neuroscience, University of Turin, Turin 10124, Italy.
8
8 Tanz Centre for Research of Neurodegenerative Diseases, Division of Neurology, Department of Medicine, University of Toronto, Toronto, Ontario M5S 3H2, Canada.
9
1 Neuromuscular Diseases Research Section, Laboratory of Neurogenetics, National Institute on Aging, Bethesda, MD 20892, USA traynorb@mail.nih.gov.
PMID:
25261972
PMCID:
PMC4240285
DOI:
10.1093/brain/awu265
[Indexed for MEDLINE]
Free PMC Article

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