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Journal: Genes, 2022
Volume: 13
Number: 2245

Article: Novel Intronic Mutation in VMA21 Causing Severe Phenotype of X-Linked Myopathy with Excessive Autophagy—Case Report
Authors: by Antoine Pegat, Nathalie Streichenberger, Nicolas Lacoste, Marc Hermier, Rita Menassa, Laurent Coudert, Julian Theuriet, Roseline Froissart, Sophie Terrone, Francoise Bouhour, Laurence Michel-Calemard, Laurent Schaeffer and Arnaud Jacquier
Link: https://www.mdpi.com/2073-4425/13/12/2245

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