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TANGO2-related rhabdomyolysis symptoms are associated with abnormal autophagy functioning

Hortense de Calbiaca Université Paris Cité, INSERM, CNRS, Institut Necker Enfants Malades, F-75015Paris, France;b Reference Center of Inherited Metabolic Diseases, Hôpital Universitaire Necker-Enfants Malades, AP-HP, Institut Imagine, Filière G2M, MetabERN, F-75015, Paris, FranceCorrespondence[email protected]
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Sebastian Montealegrea Université Paris Cité, INSERM, CNRS, Institut Necker Enfants Malades, F-75015Paris, FranceView further author information
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Marjolène Straubea Université Paris Cité, INSERM, CNRS, Institut Necker Enfants Malades, F-75015Paris, France;b Reference Center of Inherited Metabolic Diseases, Hôpital Universitaire Necker-Enfants Malades, AP-HP, Institut Imagine, Filière G2M, MetabERN, F-75015, Paris, FranceView further author information
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Solène Renaulta Université Paris Cité, INSERM, CNRS, Institut Necker Enfants Malades, F-75015Paris, France;b Reference Center of Inherited Metabolic Diseases, Hôpital Universitaire Necker-Enfants Malades, AP-HP, Institut Imagine, Filière G2M, MetabERN, F-75015, Paris, FranceView further author information
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Hugo Debrugea Université Paris Cité, INSERM, CNRS, Institut Necker Enfants Malades, F-75015Paris, France;b Reference Center of Inherited Metabolic Diseases, Hôpital Universitaire Necker-Enfants Malades, AP-HP, Institut Imagine, Filière G2M, MetabERN, F-75015, Paris, FranceView further author information
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Loïc Chentouta Université Paris Cité, INSERM, CNRS, Institut Necker Enfants Malades, F-75015Paris, France;b Reference Center of Inherited Metabolic Diseases, Hôpital Universitaire Necker-Enfants Malades, AP-HP, Institut Imagine, Filière G2M, MetabERN, F-75015, Paris, FranceView further author information
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Sorana Ciurac Translational Research for Neurological Diseases, Institut Imagine, INSERM UMR 1163, Université Paris Cité, F-75015, Paris, FranceView further author information
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Apolline Imbardd Metabolic biochemistry, Hôpital Universitaire Necker-Enfants Malades, AP-HP, Institut Imagine, Filière G2M, MetabERN, Université Paris Cité, F-75015, Paris, FranceView further author information
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Edouard Le Guilloud Metabolic biochemistry, Hôpital Universitaire Necker-Enfants Malades, AP-HP, Institut Imagine, Filière G2M, MetabERN, Université Paris Cité, F-75015, Paris, FranceView further author information
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Anca Marianc Translational Research for Neurological Diseases, Institut Imagine, INSERM UMR 1163, Université Paris Cité, F-75015, Paris, FranceView further author information
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Nicolas Goudine Cell Imaging & Flow Cytometry Core Facilities, Structure Fédérative de Recherche Necker, INSERM US24/CNRS UMS3633, F-75015, FranceView further author information
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Laure Caccavellia Université Paris Cité, INSERM, CNRS, Institut Necker Enfants Malades, F-75015Paris, France;b Reference Center of Inherited Metabolic Diseases, Hôpital Universitaire Necker-Enfants Malades, AP-HP, Institut Imagine, Filière G2M, MetabERN, F-75015, Paris, FranceView further author information
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Sylvie Fabregaf Platform, Structure Fédérative de Recherche Necker, F-75015, Paris, FranceView further author information
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Arnaud Hubasg Genetics and Molecular Biology, Laboratoire de culture cellulaire, Hôpital Universitaire Cochin, AP-HP, F-75014, Paris, FranceView further author information
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Peter van Enderta Université Paris Cité, INSERM, CNRS, Institut Necker Enfants Malades, F-75015Paris, France;h Service Immunologie Biologique, AP-HP, Hôpital Universitaire Necker-Enfants Malades, F-75015, Paris, FranceView further author information
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Nicolas Duponta Université Paris Cité, INSERM, CNRS, Institut Necker Enfants Malades, F-75015Paris, FranceView further author information
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Julien Dianaa Université Paris Cité, INSERM, CNRS, Institut Necker Enfants Malades, F-75015Paris, FranceView further author information
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Edor Kabashic Translational Research for Neurological Diseases, Institut Imagine, INSERM UMR 1163, Université Paris Cité, F-75015, Paris, FranceView further author information
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Pascale de Lonlaya Université Paris Cité, INSERM, CNRS, Institut Necker Enfants Malades, F-75015Paris, France;b Reference Center of Inherited Metabolic Diseases, Hôpital Universitaire Necker-Enfants Malades, AP-HP, Institut Imagine, Filière G2M, MetabERN, F-75015, Paris, FranceView further author information
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Article: 2306766 | Received 31 Mar 2023, Accepted 12 Jan 2024, Published online: 01 Feb 2024

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