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Acknowledgements
We thank the families who participated in this study. This work was supported by the Institut National de la Santé et de la Recherche Médicale, Centre National de la Recherche Scientifique, University of Strasbourg, the France Génomique National infrastructure, funded as part of the Investissements d’Avenir program managed by the Agence Nationale pour la Recherche (ANR-10-INBS-09), and by Fondation Maladies Rares whithin the frame of the “Myocapture” sequencing project, AFM-16992 and CREGEMES for the MYOdiagHTS project, ANR-10-LABX-0030-INRT under the frame program Investissements d’Avenir ANR-10-IDEX-0002-02, Association Française contre les Myopathies (AFM-17088).
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All procedures involving human participants were in accordance with the ethical standards of the institutional and/or national research committee and with the 1964 Helsinki declaration and its later amendments or comparable ethical standards.
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Echaniz-Laguna, A., Lornage, X., Lannes, B. et al. HSPB8 haploinsufficiency causes dominant adult-onset axial and distal myopathy. Acta Neuropathol 134, 163–165 (2017). https://doi.org/10.1007/s00401-017-1724-8
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DOI: https://doi.org/10.1007/s00401-017-1724-8