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Missense mutations of ACTA1 cause dominant congenital myopathy with cores
- Correspondence to: Angela M. Kaindl Department of Neuropediatrics, Charité, University Medical School, Augustenburger Platz 1, D-13353 Berlin, Germany; angela.kaindlcharite.de
Citation
Missense mutations of ACTA1 cause dominant congenital myopathy with cores
Publication history
- Received April 13, 2004
- Accepted April 20, 2004
- First published November 1, 2004.
Online issue publication
April 27, 2016
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Copyright 2004 Journal of Medical Genetics