Glut1 deficiency syndrome throughout life: clinical phenotypes, intelligence, life achievements and quality of life in familial cases
- Location
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Deutsche Nationalbibliothek Frankfurt am Main
- ISSN
-
1750-1172
- Extent
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Online-Ressource
- Language
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Englisch
- Notes
-
online resource.
- Bibliographic citation
-
Glut1 deficiency syndrome throughout life: clinical phenotypes, intelligence, life achievements and quality of life in familial cases ; volume:17 ; number:1 ; day:24 ; month:9 ; year:2022 ; pages:1-13 ; date:12.2022
Orphanet journal of rare diseases ; 17, Heft 1 (24.9.2022), 1-13, 12.2022
- Creator
-
Olivotto, Sara
Duse, Alessandra
Bova, Stefania Maria
Leonardi, Valeria
Biganzoli, Elia
Milanese, Alberto
Cereda, Cristina
Bertoli, Simona
Previtali, Roberto
Veggiotti, Pierangelo
- Contributor
-
SpringerLink (Online service)
- DOI
-
10.1186/s13023-022-02513-4
- URN
-
urn:nbn:de:101:1-2022121221090501557457
- Rights
-
Open Access; Der Zugriff auf das Objekt ist unbeschränkt möglich.
- Last update
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15.08.2025, 7:31 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
- Olivotto, Sara
- Duse, Alessandra
- Bova, Stefania Maria
- Leonardi, Valeria
- Biganzoli, Elia
- Milanese, Alberto
- Cereda, Cristina
- Bertoli, Simona
- Previtali, Roberto
- Veggiotti, Pierangelo
- SpringerLink (Online service)
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