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Updated: Oct 1, 2026

Modeling Myotonic Dystrophy 1 in C2C12 Myoblast Cells
Published on: July 29, 2016
Antibody deficiency in myotonic dystrophy type 1: A differential diagnosis below the radar
Edoardo Galli1,2, Christoph T Berger3, Thomas Daikeler3
1Department of Neurology, University and University Hospital of Basel, Basel, Switzerland.
Abstract:
Myotonic dystrophy type 1 is a rare, underdiagnosed genetic neuromuscular disorder that is often accompanied by hypogammaglobulinemia, serving as a crucial diagnostic clue. We report the clinical and immunophenotypic features of two patients and discuss the underlying pathogenesis.
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