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Extension of the phenotypic spectrum of GLE1‐related disord..:
Mathieu Cerino
;
Chloé Di Meglio
;
Francesca Albertini
...
https://doi.org/10.1002/mgg3.1277. , 2020
Link:
https://doi.org/10.1002/mgg3.1277
RT Journal T1
Extension of the phenotypic spectrum of GLE1‐related disorders to a mild congenital form resembling congenital myopathy
UL https://suche.suub.uni-bremen.de/peid=base-ftdoajarticles:oai:doaj.org_article:05ff4f1ca3fe4f7e8fead30f22799de0&Exemplar=1&LAN=DE A1 Mathieu Cerino A1 Chloé Di Meglio A1 Francesca Albertini A1 Frédérique Audic A1 Florence Riccardi A1 Christophe Boulay A1 Nicole Philip A1 Marc Bartoli A1 Nicolas Lévy A1 Martin Krahn A1 Brigitte Chabrol PB Wiley YR 2020 K1 congenital K1 GLE1 K1 mild K1 mutation K1 myopathy K1 NGS K1 Genetics K1 QH426-470 JF https://doi.org/10.1002/mgg3.1277 LK http://dx.doi.org/https://doi.org/10.1002/mgg3.1277 DO https://doi.org/10.1002/mgg3.1277 SF ELIB - SuUB Bremen
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