EIF2B2 gene mutation causing early onset vanishing white matter disease: a case report
- Location
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Deutsche Nationalbibliothek Frankfurt am Main
- ISSN
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1824-7288
- Extent
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Online-Ressource
- Language
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Englisch
- Notes
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online resource.
- Bibliographic citation
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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
- Creator
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Filareto, Ilaria
Cinelli, Giulia
Scalabrini, Ilaria
Caramaschi, Elisa
Bergonzini, Patrizia
Spezia, Elisabetta
Todeschini, Alessandra
Iughetti, Lorenzo
- Contributor
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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
- Rights
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Open Access; Der Zugriff auf das Objekt ist unbeschränkt möglich.
- Last update
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15.08.2025, 7:39 AM CEST
Data provider
This object is provided by:
Deutsche Nationalbibliothek. If you have any questions about the object, please contact the data provider.
Deutsche Nationalbibliothek. If you have any questions about the object, please contact the data provider.
Associated
- Filareto, Ilaria
- Cinelli, Giulia
- Scalabrini, Ilaria
- Caramaschi, Elisa
- Bergonzini, Patrizia
- Spezia, Elisabetta
- Todeschini, Alessandra
- Iughetti, Lorenzo
- SpringerLink (Online service)
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