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Authors
Labasse, Clémence
Brochier, Guy
Taratuto, Ana-Lia
Cadot, Bruno
Rendu, John
Monges, Soledad
Biancalana, Valérie
Quijano-Roy, Susana
Bui, Mai Thao
Chanut, Anaïs
Madelaine, Angéline
Lacène, Emmanuelle
Beuvin, Maud
Amthor, Helge
Servais, Laurent
de Feraudy, Yvan
Erro, Marcela
Saccoliti, Maria
Neto, Osorio Abath
Fauré, Julien
Lannes, Béatrice
Laugel, Vincent
Coppens, Sandra
Lubieniecki, Fabiana
Bello, Ana Buj
Laing, Nigel
Evangelista, Teresinha
Laporte, Jocelyn
Böhm, Johann
Romero, Norma B. https://orcid.org/0000-0001-7714-0069
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Funding
Funding for this research was provided by:
Association Française contre les Myopathies (AFM-22734)
Association Institute of Myology
Fondation Maladies Rares
France Génomique ((ANR-10-INBS-09))
Australian National Health and Medical Research Council
Inserm, CNRS, University of Strasbourg
Society for the Study of Artificial Intelligence and the Simulation of Behaviour
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Article History
Received: 17 June 2022
Accepted: 19 June 2022
First Online: 9 July 2022
Declarations
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: Molecular diagnosis was carried out with written informed consent from the patients or legal guardians. DNA storage and usage were IRB-approved (DC-2012–1693).
: All patients and legal guardians’ consent to the publication of the clinical, histological, and genetic data.
: None of the authors reports a conflict of interests.
