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Missense mutations of ACTA1 cause dominant congenital myopathy with cores
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  1. Correspondence to:
 Angela M. Kaindl
 Department of Neuropediatrics, Charité, University Medical School, Augustenburger Platz 1, D-13353 Berlin, Germany; angela.kaindlcharite.de
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Citation

Kaindl AM, Rüschendorf F, Krause S, et al
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 
November 01, 2004

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