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Feldkirchner, S., Walter, M. C., Kubny, C., Mueller, S., Kress, W., Hanisch, F. G., Schoser, B. and Schessl, J. (2011). The C224W FHL1 mutation is causing a protein aggregation disorder of muscle: Two brothers revisited. Neuromusc. Disord., 21 (9-10). S. 740 - 741. OXFORD: PERGAMON-ELSEVIER SCIENCE LTD. ISSN 0960-8966
Schessl, J., Bach, E., Rost, S., Feldkirchner, S., Kubny, C., Mueller, S., Hanisch, F. G., Kress, W. and Schoser, B. (2014). Novel recessive myotilin mutation cause severe myofibrillar myopathy. Neuromusc. Disord., 24 (9-10). S. 832 - 833. OXFORD: PERGAMON-ELSEVIER SCIENCE LTD. ISSN 1873-2364