A Mutation in the Dimerization Domain of Filamin C Causes a Novel Type of Autosomal Dominant Myofibrillar Myopathy
Title:
A Mutation in the Dimerization Domain of Filamin C Causes a Novel Type of Autosomal Dominant Myofibrillar Myopathy
Author:
Vorgerd, Matthias van der Ven, Peter F.M. Bruchertseifer, Vera Löwe, Thomas Kley, Rudolf A. Schröder, Rolf Lochmüller, Hanns Himmel, Mirko Koehler, Katrin Fürst, Dieter O. Huebner, Angela