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S Rudnik-Schoeneborn
S Rudnik-Schoeneborn
RWTH Aachen University
Biology
Genetics
Spinal muscular atrophy
Diabetes mellitus
Cognition
2
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P.159Disease spectrum in nemaline myopathy due to LMOD3 mild founder mutation in Austria and southern Germany
2019
Neuromuscular Disorders
Scott L. Weiss
Ulrich A. Schatz
J. Zschoke
Stephan Wenninger
Benedikt Schoser
S Rudnik-Schoeneborn
W. Muss
Anna Schossig
Wolfgang M. Schmidt
Reginald E. Bittner
G. Bernert
Matthias Baumann
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Response to comments by J.S. Sieratzki and B. Woll: Cognitive function in children with spinal muscular atrophy
2002
Neuromuscular Disorders
A. von Gontard
S Rudnik-Schoeneborn
Klaus Zerres
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