Expanding SPG18 clinical spectrum: autosomal dominant mutation causes complicated hereditary spastic paraplegia in a large family
- Standort
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Deutsche Nationalbibliothek Frankfurt am Main
- Umfang
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1 Online-Ressource.
- Sprache
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Englisch
- Erschienen in
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Expanding SPG18 clinical spectrum: autosomal dominant mutation causes complicated hereditary spastic paraplegia in a large family ; day:12 ; month:4 ; year:2024 ; pages:1-9
Neurological sciences ; (12.4.2024), 1-9
- Urheber
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Trinchillo, Assunta
Valente, Valeria
Esposito, Marcello
Migliaccio, Miriana
Iovino, Aniello
Picciocchi, Michele
Cuomo, Nunzia
Caccavale, Carmela
Nocerino, Cristofaro
Rosa, Laura De
Salvatore, Elena
Pierantoni, Giovanna Maria
Menchise, Valeria
Paladino, Simona
Criscuolo, Chiara
- Beteiligte Personen und Organisationen
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SpringerLink (Online service)
- DOI
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10.1007/s10072-024-07500-0
- URN
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urn:nbn:de:101:1-2406252100131.203270016504
- Rechteinformation
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Open Access; Der Zugriff auf das Objekt ist unbeschränkt möglich.
- Letzte Aktualisierung
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14.08.2025, 11:00 MESZ
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Beteiligte
- Trinchillo, Assunta
- Valente, Valeria
- Esposito, Marcello
- Migliaccio, Miriana
- Iovino, Aniello
- Picciocchi, Michele
- Cuomo, Nunzia
- Caccavale, Carmela
- Nocerino, Cristofaro
- Rosa, Laura De
- Salvatore, Elena
- Pierantoni, Giovanna Maria
- Menchise, Valeria
- Paladino, Simona
- Criscuolo, Chiara
- SpringerLink (Online service)
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