Glut1 deficiency syndrome throughout life: clinical phenotypes, intelligence, life achievements and quality of life in familial cases
- Standort
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Deutsche Nationalbibliothek Frankfurt am Main
- ISSN
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1750-1172
- 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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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
- Urheber
-
Olivotto, Sara
Duse, Alessandra
Bova, Stefania Maria
Leonardi, Valeria
Biganzoli, Elia
Milanese, Alberto
Cereda, Cristina
Bertoli, Simona
Previtali, Roberto
Veggiotti, Pierangelo
- Beteiligte Personen und Organisationen
-
SpringerLink (Online service)
- DOI
-
10.1186/s13023-022-02513-4
- URN
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urn:nbn:de:101:1-2022121221090501557457
- Rechteinformation
-
Open Access; Der Zugriff auf das Objekt ist unbeschränkt möglich.
- Letzte Aktualisierung
-
15.08.2025, 07:31 MESZ
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Beteiligte
- 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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