Thomas Löwe

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.