Extension of the phenotypic spectrum of GLE1 ‐related disorders to a mild congenital form resembling congenital myopathy - Aix-Marseille Université Access content directly
Journal Articles Molecular Genetics & Genomic Medicine Year : 2020

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

Chloé Di Meglio
  • Function : Author
Francesca Albertini
  • Function : Author
Frédérique Audic
  • Function : Author
Christophe Boulay
  • Function : Author

Dates and versions

hal-03222418 , version 1 (10-05-2021)

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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, 2020, 8 (8), ⟨10.1002/mgg3.1277⟩. ⟨hal-03222418⟩
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