EIF2B2 gene mutation causing early onset vanishing white matter disease: a case report
- Standort
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Deutsche Nationalbibliothek Frankfurt am Main
- ISSN
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1824-7288
- Umfang
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Online-Ressource
- Sprache
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Englisch
- Anmerkungen
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online resource.
- Erschienen in
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EIF2B2 gene mutation causing early onset vanishing white matter disease: a case report ; volume:48 ; number:1 ; day:27 ; month:7 ; year:2022 ; pages:1-9 ; date:12.2022
The Italian journal of pediatrics ; 48, Heft 1 (27.7.2022), 1-9, 12.2022
- Urheber
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Filareto, Ilaria
Cinelli, Giulia
Scalabrini, Ilaria
Caramaschi, Elisa
Bergonzini, Patrizia
Spezia, Elisabetta
Todeschini, Alessandra
Iughetti, Lorenzo
- Beteiligte Personen und Organisationen
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SpringerLink (Online service)
- DOI
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10.1186/s13052-022-01325-3
- URN
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urn:nbn:de:101:1-2022100820273445404122
- Rechteinformation
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Open Access; Der Zugriff auf das Objekt ist unbeschränkt möglich.
- Letzte Aktualisierung
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15.08.2025, 07:39 MESZ
Datenpartner
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Beteiligte
- Filareto, Ilaria
- Cinelli, Giulia
- Scalabrini, Ilaria
- Caramaschi, Elisa
- Bergonzini, Patrizia
- Spezia, Elisabetta
- Todeschini, Alessandra
- Iughetti, Lorenzo
- SpringerLink (Online service)
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