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Modeling Myotonic Dystrophy 1 in C2C12 Myoblast Cells
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Lower extremity muscle pathology in myotonic dystrophy type 1 assessed by quantitative MRI

Linda Heskamp1, Marlies van Nimwegen2, Marieke J Ploegmakers2

  • 1From the Department of Radiology and Nuclear Medicine (L.H., M.J.P., A.H.) and Department of Neurology (M.v.N., B.G.M.v.E.), Radboud University Medical Center, Nijmegen, the Netherlands; Neuromuscular Reference Center (G.B.), Sorbonne University, INSERM UMRS 974, AP-HP, Pitié-Salpêtrière Hospital; Department of Radiology (J.-F.D.), Henri Mondor University Hospital, Paris, France; and Institute of Molecular, Cell and Systems Biology (S.A.C., D.G.M.), College of Medical, Veterinary and Life Sciences, University of Glasgow, UK. linda.heskamp@radboudumc.nl.

Neurology
|May 24, 2019
PubMed
Abstract

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