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Up to: Hereditary neurological disease · Neuromuscular disease caused by qualitative or quantitative defects of myofibrillar proteins

Qualitative or quantitative defects of desmin

0 trials tagged with this condition →

  • Rigid spine syndrome 0 trials · 1 incl. sub-types Sub-types →
  • Autosomal dominant limb-girdle muscular dystrophy type 1E (DES) 0 trials
  • Dilated cardiomyopathy 1I 0 trials
  • Myofibrillar myopathy 1 0 trials
  • Neurogenic scapuloperoneal syndrome, Kaeser type 0 trials

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