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A Mutation in the Dimerization Domain of Filamin C Causes a Novel Type of Autosomal Dominant Myofibrillar Myopathy Matthias Vorgerd, Peter F.M. van der.

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Presentation on theme: "A Mutation in the Dimerization Domain of Filamin C Causes a Novel Type of Autosomal Dominant Myofibrillar Myopathy Matthias Vorgerd, Peter F.M. van der."— Presentation transcript:

1 A Mutation in the Dimerization Domain of Filamin C Causes a Novel Type of Autosomal Dominant Myofibrillar Myopathy 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 The American Journal of Human Genetics Volume 77, Issue 2, Pages 297-304 (August 2005) DOI: 10.1086/431959 Copyright © 2005 The American Society of Human Genetics Terms and Conditions Terms and Conditions

2 Figure 1 The American Journal of Human Genetics 2005 77, 297-304DOI: (10.1086/431959) Copyright © 2005 The American Society of Human Genetics Terms and Conditions Terms and Conditions

3 Figure 2 The American Journal of Human Genetics 2005 77, 297-304DOI: (10.1086/431959) Copyright © 2005 The American Society of Human Genetics Terms and Conditions Terms and Conditions

4 Figure 3 The American Journal of Human Genetics 2005 77, 297-304DOI: (10.1086/431959) Copyright © 2005 The American Society of Human Genetics Terms and Conditions Terms and Conditions

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