Benedikt Schoser is senior consultant at the Friedrich-Baur-Institute, Dept. of Neurology at the Ludwig-Maximilians-University of Munich, Germany. He is coordinator of the diagnostic working group within the German MD-NET, member of the German reference group for neuromuscular disorders, and TREAT-NMD. Benedikt Schoser has a long-standing interest in the pathogenesis of muscular dystrophies, myotonic dystrophies, and metabolic myopathies. He is engaged in all types of morphological and molecular analyses including animal models and human myoblast cell culture studies. He has a special interest in translational therapy of myotonic dystrophies and glycogen storage disorders.
Article first published online: 17 JAN 2012
Copyright © 2012 Wiley Periodicals, Inc.
American Journal of Medical Genetics Part C: Seminars in Medical Genetics
Special Issue: Advancements in Pompe Disease
Volume 160C, Issue 1, pages 80–88, 15 February 2012
How to Cite
Schüller, A., Wenninger, S., Strigl-Pill, N. and Schoser, B. (2012), Toward deconstructing the phenotype of late-onset Pompe disease. Am. J. Med. Genet., 160C: 80–88. doi: 10.1002/ajmg.c.31322
Doctors Angela Schüller, Stephan Wenninger, and Nicola Strigl-Pill are members of Dr. Schoseŕs working group at the Friedrich-Baur-Institute.
How to cite this article: Schüller A, Wenninger S, Strigl-Pill N, Schoser B. 2012. Toward deconstructing the phenotype of late-onset Pompe disease. Am J Med Genet Part C Semin Med Genet 160C:80–88.
- Issue published online: 23 JAN 2012
- Article first published online: 17 JAN 2012
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