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Authors
Feichtinger, René G.
Mucha, Bettina E.
Hengel, Holger
Orfi, Zakaria
Makowski, Christine
Dort, Junio
D’Anjou, Guy
Nguyen, Thi Tuyet Mai
Buchert, Rebecca
Juenger, Hendrik
Freisinger, Peter
Baumeister, Sarah
Schoser, Benedikt
Ahting, Uwe
Keimer, Reinhard
Nguyen, Cam-Tu Emilie
Fabre, Paul
Gauthier, Julie
Miguet, Marguerite
Lopes, Fátima
AlHakeem, Afnan
AlHashem, Amal
Tabarki, Brahim
Kandaswamy, Krishna Kumar
Bauer, Peter
Steinbacher, Peter
Prokisch, Holger
Sturm, Marc
Strom, Tim M.
Ellezam, Benjamin
Mayr, Johannes A.
Schöls, Ludger
Michaud, Jacques L.
Campeau, Philippe M.
Haack, Tobias B.
Dumont, Nicolas A.
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Funding
Funding for this research was provided by:
Bundesministerium für Bildung und Forschung (FKZ01ZX1405C)
Horizon 2020 (01GM1603 and 01GM1207)
Horizon 2020 (FWFI2741B26)
Deutsche Forschungsgemeinschaft (SCHO754/52)
Deutsche Forschungsgemeinschaft (BA2427/22)
EU FP7 Mitochondrial European Educational Training Project (317433)
Horizon 2020 (633974)
Fonds de Recherche du Québec - Santé (35015)
Canadian Institutes of Health Research (388296)
Rare Disease Foundation (2301)
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More Information
This article is maintained by: Elsevier
Article Title: Biallelic variants in the transcription factor PAX7 are a new genetic cause of myopathy
Journal Title: Genetics in Medicine
CrossRef DOI link to publisher maintained version: https://doi.org/10.1038/s41436-019-0532-z
Content Type: article
Copyright: © 2019, The Author(s), under exclusive licence to the American College of Medical Genetics and Genomics
