Exome sequencing reveals DNAJB6 mutations in dominantly-inherited myopathy
Version of Record online: 14 FEB 2012
Copyright © 2012 American Neurological Association
Annals of Neurology
Volume 71, Issue 3, pages 407–416, March 2012
How to Cite
Harms, M. B., Sommerville, R. B., Allred, P., Bell, S., Ma, D., Cooper, P., Lopate, G., Pestronk, A., Weihl, C. C. and Baloh, R. H. (2012), Exome sequencing reveals DNAJB6 mutations in dominantly-inherited myopathy. Ann Neurol., 71: 407–416. doi: 10.1002/ana.22683
- Issue online: 23 MAR 2012
- Version of Record online: 14 FEB 2012
- Accepted manuscript online: 27 NOV 2011 11:11PM EST
- Manuscript Accepted: 18 NOV 2011
- Manuscript Revised: 23 OCT 2011
- Manuscript Received: 7 SEP 2011
- BJC Institute for Clinical and Translational Sciences
- Children's Discovery Institute, National Institutes of Health (NIH). Grant Numbers: NINDS NS055980, NS069669, NINDS NS075094, NIA AG031867
- Neuroscience Blueprint Core Grant. Grant Number: NS057105
- Hope Center for Neurological Disorders
- Muscular Dystrophy Association. Grant Numbers: 35438, 114845
- Burroughs Wellcome Fund
- Siteman Cancer Center. Grant Number: P30 CA91842
- National Center for Research Resources (NCRR), a component of the National Institutes of Health (NIH), and NIH Roadmap for Medical Research. Grant Number: UL1RR024992
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