Amyotrophic lateral sclerosis associated with a pathological expansion in the ATXN7 gene

Author:

Cluse Florent12,Bernard Emilien123ORCID,Strubi-Vuillaume Isabelle4,Devos David5ORCID,Mouzat Kevin6,Lumbroso Serge6,Froment Tilikete Caroline789,Thobois StÉphane11011,Pegat Antoine12

Affiliation:

1. ALS Resource and Competence Centre, Pierre Wertheimer Hospital, Hospices Civils de Lyon, Bron, France

2. Electroneuromyography and Neuromuscular Diseases Unit, Pierre Wertheimer Hospital, Hospices Civils de Lyon, Bron, France

3. NeuroMyoGène Institute, CNRS UMR5310, INSERM U1217, University of Lyon I, Lyon, France

4. Biology and Pathology Centre, University Hospital of Lille, Lille, France

5. Department of Pharmacology, LiCEND, ALS Expert Center, University Hospital of Lille, University of Lille, Lille Neuroscience & Cognition, Inserm U1172, Lille, France

6. Laboratory of Biochemistry and Molecular Biology, University Hospital of Nîmes, Nîmes, Motoneuron Disease: Pathophysiology and Therapy, INM, University of Montpellier, Montpellier, France

7. Neuro-ophtalmology and Neuro-cognition Unit, Pierre Wertheimer Hospital, Hospices Civils de Lyon, Bron, France

8. Faculté de médecine Lyon Est, University of Lyon, Lyon, France

9. Lyon Neuroscience Research Center, INSERM U1028 CNRS UMR 5292, Team impact, Bron, France

10. Faculté de médecine et de Maïeutique Lyon Sud Charles Mérieux, University of Lyon, Lyon, France, and

11. CNRS, Institut des Sciences Cognitives Marc Jeannerod, UMR 5229, Bron, France.

Publisher

Informa UK Limited

Subject

Neurology (clinical),Neurology

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