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Letters to JMG
Missense mutations of ACTA1 cause dominant congenital myopathy with cores

https://doi.org/10.1136/jmg.2004.020271

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    Footnotes

    • This work was supported by the German Ministry of Education and Research (BMBF, Bonn, Germany), the Myositis Association (Harrisonburg, VA, USA), and the MeDDrive program (Technical University Dresden, Germany). FR, CB, and PN are supported by the German Genome Research Network (NGFN).

    • Conflict of interest: none declared.