A.P.5
Schessl, J, Bach, E, Rost, S, Feldkirchner, S, Kubny, C, Müller, S, Hanisch, F.G, Kress, W, Schoser, B
Published in Neuromuscular disorders : NMD (01.10.2014)
Published in Neuromuscular disorders : NMD (01.10.2014)
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Journal Article
G.P.123 Identification of molecular effects of FHL1 mutations on protein assembly in reducing body myopathy
Kubny, C, Bulst, S, Levin, J, Krause, S, Schoser, B, Giese, A, Walter, M.C, Schessl, J
Published in Neuromuscular disorders : NMD (01.10.2012)
Published in Neuromuscular disorders : NMD (01.10.2012)
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Journal Article
P5.53 The C224W FHL1 mutation is causing a protein aggregation disorder of muscle: Two brothers revisited
Feldkirchner, S, Walter, M.C, Kubny, C, Mueller, S, Kress, W, Hanisch, F.G, Schoser, B, Schessl, J
Published in Neuromuscular disorders : NMD (01.10.2011)
Published in Neuromuscular disorders : NMD (01.10.2011)
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Journal Article
P2.42 Cys150Arg FHL1 mutation in two brothers affected by the Emery-Dreifuss muscular dystrophy phenotype
Ortez, C, Nascimento, A, Jimenez-Mallabrera, C, Feldkirchner, S, Kubny, C, Schessl, J, Jou, C, Corbera, J, Roig, M, Colomer, J
Published in Neuromuscular disorders : NMD (01.10.2011)
Published in Neuromuscular disorders : NMD (01.10.2011)
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Journal Article
A.P.5: Novel recessive myotilin mutation cause severe myofibrillar myopathy
Schessl, J., Bach, E., Rost, S., Feldkirchner, S., Kubny, C., Müller, S., Hanisch, F.G., Kress, W., Schoser, B.
Published in Neuromuscular disorders : NMD (01.10.2014)
Published in Neuromuscular disorders : NMD (01.10.2014)
Get full text
Journal Article