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

BACKGROUND: GLE1 (GLE1, RNA Export Mediator, OMIM#603371) variants are associated with severe autosomal recessive motor neuron diseases, that are lethal congenital contracture syndrome 1 (LCCS1, OMIM#253310) and congenital arthrogryposis with anterior horn cell disease (CAAHD, OMIM#611890). The clin...

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Detalles Bibliográficos
Autores principales: Cerino, Mathieu, Di Meglio, Chloé, Albertini, Francesca, Audic, Frédérique, Riccardi, Florence, Boulay, Christophe, Philip, Nicole, Bartoli, Marc, Lévy, Nicolas, Krahn, Martin, Chabrol, Brigitte
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2020
Materias:
Clinical Reports
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7434744/
https://www.ncbi.nlm.nih.gov/pubmed/32537934
http://dx.doi.org/10.1002/mgg3.1277

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7434744/
https://www.ncbi.nlm.nih.gov/pubmed/32537934
http://dx.doi.org/10.1002/mgg3.1277

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