Missense mutations of ACTA1 cause dominant congenital myopathy with cores. Issue 11 (1st November 2004) - Kaindl, A M; Rüschendorf, F; Krause, S; Goebel, H-H; Koehler, K; Becker, C; Pongratz, D; Müller-Höcker, J; Nürnberg, P; Stoltenburg-Didinger, G; Lochmüller, H; Huebner, A