Molecular Genetics and Metabolism Reports (Mar 2024)
New mutations identified in a case of Glycogenin-1 deficiency
- R. Pruvost,
- M. Csanyi,
- G. Lefebvre,
- V. Biancalana,
- E. Malfatti,
- F. Cassim,
- C. Oldfors,
- L. Defebvre,
- A. Oldfors,
- C. Tard
Affiliations
- R. Pruvost
- Department of Movement Disorder and NS-PARK/centre de référence des maladies neuromusculaires Nord/Est/Ile-de-France, Inserm 1172 University of Lille, Lille, France; Corresponding author.
- M. Csanyi
- Department of Pathology, Lille Universitary Hospital Center, Lille, France
- G. Lefebvre
- Musculoskeletal Imaging Department, Centre de Consultation et d'Imagerie de l'Appareil Locomoteur, CHU Lille, University of Lille Nord de France, F-59000, Lille, France
- V. Biancalana
- Laboratory of Diagnostic Genetics, Faculty of Medicine, University of Strasbourg, France
- E. Malfatti
- Biology of the Neuromuscular System, University Paris-Est Créteil, INSERM, U955 IMRB, F-94010 Créteil, France
- F. Cassim
- Department of Movement Disorder and NS-PARK/centre de référence des maladies neuromusculaires Nord/Est/Ile-de-France, Inserm 1172 University of Lille, Lille, France
- C. Oldfors
- Department of Pathology, Sahlgrenska University Hospital, Goteborg, Sweden
- L. Defebvre
- Department of Movement Disorder and NS-PARK/centre de référence des maladies neuromusculaires Nord/Est/Ile-de-France, Inserm 1172 University of Lille, Lille, France
- A. Oldfors
- Department of Pathology, Sahlgrenska University Hospital, Goteborg, Sweden
- C. Tard
- Department of Movement Disorder and NS-PARK/centre de référence des maladies neuromusculaires Nord/Est/Ile-de-France, Inserm 1172 University of Lille, Lille, France
- Journal volume & issue
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Vol. 38
p. 101046