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Journal Article
Schessl, Joachim, Bach, Elisa, Rost, Simone, Feldkirchner, Sarah, Kubny, Christiana, Mueller, Stefan, Hanisch, Franz-Georg, Kress, Wolfram and Schoser, Benedikt 
ORCID: 0000-0002-2757-8131
(2014).
Novel recessive myotilin mutation causes severe myofibrillar myopathy.
Neurogenetics, 15 (3).
S. 151 - 157.
NEW YORK:
SPRINGER.
ISSN 1364-6753
Feldkirchner, Sarah, Schessl, Joachim, Mueller, Stefan, Schoser, Benedikt ORCID: 0000-0002-2757-8131 and Hanisch, Franz-Georg
(2012).
Patient-specific protein aggregates in myofibrillar myopathies: Laser microdissection and differential proteomics for identification of plaque components.
Proteomics, 12 (23-24).
S. 3598 - 3610.
HOBOKEN:
WILEY-BLACKWELL.
ISSN 1615-9853
Clemen, Christoph S., Tangavelou, Karthikeyan, Strucksberg, Karl-Heinz, Just, Steffen, Gaertner, Linda, Regus-Leidig, Hanna, Stumpf, Maria, Reimann, Jens, Coras, Roland, Morgan, Reginald O. ORCID: 0000-0002-2059-792X, Fernandez, Maria-Pilar, Hofmann, Andreas ORCID: 0000-0003-4408-5467, Mueller, Stefan, Schoser, Benedikt ORCID: 0000-0002-2757-8131, Hanisch, Franz-Georg, Rottbauer, Wolfgang, Bluemcke, Ingmar, von Hoersten, Stephan, Eichinger, Ludwig ORCID: 0000-0003-1594-6117 and Schroeder, Rolf
(2010).
Strumpellin is a novel valosin-containing protein binding partner linking hereditary spastic paraplegia to protein aggregation diseases.
Brain, 133.
S. 2920 - 2942.
OXFORD:
OXFORD UNIV PRESS.
ISSN 1460-2156