Foetal onset of EIF2B related disorder in two siblings: cerebellar hypoplasia with absent Bergmann glia and severe hypomyelination
- Standort
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Deutsche Nationalbibliothek Frankfurt am Main
- ISSN
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2051-5960
- Umfang
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Online-Ressource
- Sprache
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Englisch
- Anmerkungen
-
online resource.
- Erschienen in
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Foetal onset of EIF2B related disorder in two siblings: cerebellar hypoplasia with absent Bergmann glia and severe hypomyelination ; volume:8 ; number:1 ; day:15 ; month:4 ; year:2020 ; pages:1-7 ; date:12.2020
Acta Neuropathologica Communications ; 8, Heft 1 (15.4.2020), 1-7, 12.2020
- Urheber
-
Trimouille, Aurélien
Marguet, Florent
Sauvestre, Fanny
Lasseaux, Eulalie
Pelluard, Fanny
Martin-Négrier, Marie-Laure
Plaisant, Claudio
Rooryck, Caroline
Lacombe, Didier
Arveiler, Benoît
Boespflug-Tanguy, Odile
Naudion, Sophie
Laquerrière, Annie
- Beteiligte Personen und Organisationen
-
SpringerLink (Online service)
- DOI
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10.1186/s40478-020-00929-2
- URN
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urn:nbn:de:101:1-2020062814563971811971
- Rechteinformation
-
Open Access; Der Zugriff auf das Objekt ist unbeschränkt möglich.
- Letzte Aktualisierung
-
14.08.2025, 10:49 MESZ
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Beteiligte
- Trimouille, Aurélien
- Marguet, Florent
- Sauvestre, Fanny
- Lasseaux, Eulalie
- Pelluard, Fanny
- Martin-Négrier, Marie-Laure
- Plaisant, Claudio
- Rooryck, Caroline
- Lacombe, Didier
- Arveiler, Benoît
- Boespflug-Tanguy, Odile
- Naudion, Sophie
- Laquerrière, Annie
- SpringerLink (Online service)
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