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. 2004 Nov;41(11):842-8.
doi: 10.1136/jmg.2004.020271.

Missense mutations of ACTA1 cause dominant congenital myopathy with cores

A M Kaindl, F Rüschendorf, S Krause, H-H Goebel, K Koehler, C Becker, D Pongratz, J Müller-Höcker, P Nürnberg, G Stoltenburg-Didinger, H Lochmüller, A Huebner

Missense mutations of ACTA1 cause dominant congenital myopathy with cores

A M Kaindl et al. J Med Genet. 2004 Nov.
No abstract available

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