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Titre
Further delineation of a rare recessive encephalomyopathy linked to mutations in GFER thanks to data sharing of whole exome sequencing data
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BSO - Titre
Further delineation of a rare recessive encephalomyopathy linked to mutations in GFER thanks to data sharing of whole exome sequencing data
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DOI
DOI
10.1111/cge.12985
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DOAI
DOAI
10.1111/cge.12985
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Identifiant WoS
WOS:000405588000009
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Accès ouvert
OA - Non
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Source - Accès ouvert
OA - Non
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Type d'accès
Non OA
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Editeur
Wiley
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Source
CLINICAL GENETICS
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ISSN
0009-9163
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Type de document
Article
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Notoriété
3 - Correcte
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CNRS
Oui
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CNRS - Institut
INSB - Institut des sciences biologiques
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uid:/0VSRTRD7
12/10/2021 14:52:47 (latest)
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