Dominant Mutations in KBTBD13, a Member of the BTB/Kelch Family, Cause Nemaline Myopathy with Cores
- 10 December 2010
- journal article
- research article
- Published by Elsevier BV in American Journal of Human Genetics
- Vol. 87 (6), 842-847
- https://doi.org/10.1016/j.ajhg.2010.10.020
Abstract
No abstract availableFunding Information
- Uniformed Services University of the Health Sciences (PI08-574)
- National Health and Medical Research Council (403904, 403941)
- National Institutes of Health
- Instituto de Salud Carlos III
- Consejería de Educación e Investigación
- National Institute of Neurological Disorders and Stroke
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