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A Mutation in the Dimerization Domain of Filamin C Causes a Novel Type of Autosomal Dominant Myofibrillar Myopathy

Author:

Matthias Vorgerd,Peter F.M. van der Ven,Vera Bruchertseifer,Thomas Löwe,Rudolf A. Kley,Rolf Schröder,Hanns Lochmüller,Mirko Himmel,Katrin Koehler,Dieter O. Fürst,Angela Huebner

Publication:

The American Journal of Human Genetics

Publisher:

Elsevier

Date:

August 2005

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