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Number of items: 3.

Journal Article

Feldkirchner, S., Mueller, S., Kress, W., Hanisch, F. G., Schoser, B. and Schessl, J. (2011). Evaluation of standardized protein pattern of skeletal muscle fibers via laser microdissection. Neuromusc. Disord., 21 (9-10). S. 739 - 741. OXFORD: PERGAMON-ELSEVIER SCIENCE LTD. ISSN 0960-8966

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

This list was generated on Mon Oct 25 06:27:45 2021 CEST.