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Extension of the phenotypic spectrum of GLE1 ‐related disorders to a mild congenital form resembling congenital myopathy

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https://hal-amu.archives-ouvertes.fr/hal-03222418
Contributor : Valérie Gall <>
Submitted on : Monday, May 10, 2021 - 11:32:43 AM
Last modification on : Tuesday, May 11, 2021 - 3:15:29 AM

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Mathieu Cerino, Chloé Di Meglio, Francesca Albertini, Frédérique Audic, Florence Riccardi, et al.. Extension of the phenotypic spectrum of GLE1 ‐related disorders to a mild congenital form resembling congenital myopathy. Molecular Genetics & Genomic Medicine, Wiley Periodicals, Inc. 2020, 8 (8), ⟨10.1002/mgg3.1277⟩. ⟨hal-03222418⟩

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