Extension of the phenotypic spectrum of GLE1‐related disorders to a mild congenital form resembling congenital myopathy by Mathieu Cerino, Chloé Di Meglio, Francesca Albertini, Frédérique Audic, Florence Riccardi, Christophe Boulay, Nicole Philip, Marc Bartoli, Nicolas Lévy, Martin Krahn, Brigitte Chabrol

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