Novel Intronic Mutation in <i>VMA21</i> Causing Severe Phenotype of X-Linked Myopathy with Excessive Autophagy—Case Report 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, Arnaud Jacquier

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