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Titre
Novel UBQLN2 mutations linked to amyotrophic lateral sclerosis and atypical hereditary spastic paraplegia phenotype through defective HSP70-mediated proteolysis
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BSO - Titre
Novel UBQLN2 mutations linked to amyotrophic lateral sclerosis and atypical hereditary spastic paraplegia phenotype through defective HSP70-mediated proteolysis
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DOI
DOI
10.1016/j.neurobiolaging.2017.06.018
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DOAI
DOAI
10.1016/j.neurobiolaging.2017.06.018
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Identifiant WoS
WOS:000408703300025
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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
Elsevier
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Source
NEUROBIOLOGY OF AGING
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ISSN
0197-4580
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Type de document
Article
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Notoriété
4 - Excellente
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CNRS
Oui
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CNRS - Institut
INSB - Institut des sciences biologiques
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uid:/3SHT1RL4
12/10/2021 14:52:50 (latest)
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