Peter F M van der Ven

A Combined Laser Microdissection and Mass Spectrometry Approach Reveals New Disease Relevant Proteins Accumulating in Aggregates of Filaminopathy Patients*

Christian Stephan, Katrin Marcus, Martin Tegenthoff, 2012, Molecular & Cellular Proteomics.

New cardiac and skeletal protein aggregate myopathy associated with combined MuRF1 and MuRF3 mutations.

Isidro Ferrer, Laura González, Benjamín Torrejón-Escribano, 2015, Human molecular genetics.

Xin repeats define a novel actin-binding motif

Klemens Rottner, Theresia Stradal, K. Rottner, 2004, Journal of Cell Science.

A mutation in the dimerization domain of filamin c causes a novel type of autosomal dominant myofibrillar myopathy.

Hanns Lochmüller, Rolf Schröder, M. Vorgerd, 2005, American journal of human genetics.