[Metabolic dysfunctions in type I myotonic dystrophy: A potential therapeutic target]

Lola Lessard1, Laure Gallay2, Rémi Mounier3

  • 1Institut NeuroMyoGène, Laboratoire Physiopathologie et Génétique du Neurone et du Muscle, CNRS UMR 5261 - Inserm U1315, Université Claude Bernard Lyon 1, Lyon, France - Département des pathologies neuromusculaires, Hôpital Neurologique Pierre Wertheimer, Hospices Civils de Lyon, France.

Medecine Sciences : M/S
|November 18, 2024
PubMed

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