C. Kubny

Novel recessive myotilin mutation causes severe myofibrillar myopathy

J. Schessl, W. Kress, B. Schoser, 2014, neurogenetics.

Reducing body myopathy and other FHL1-related muscular disorders.

J. Schessl, B. Schoser, S. Feldkirchner, 2011, Seminars in pediatric neurology.

Novel recessive myotilin mutation causes severe myofibrillar myopathy

J. Schessl, W. Kress, B. Schoser, 2014, neurogenetics.

Proteomic characterization of aggregate components in an intrafamilial variable FHL1-associated myopathy

J. Schessl, W. Kress, B. Schoser, 2013, Neuromuscular Disorders.