Whole-exome sequencing confirms implication of VPS13D as a potential cause of progressive spastic ataxia
- Standort
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Deutsche Nationalbibliothek Frankfurt am Main
- ISSN
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1471-2377
- 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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Whole-exome sequencing confirms implication of VPS13D as a potential cause of progressive spastic ataxia ; volume:22 ; number:1 ; day:12 ; month:2 ; year:2022 ; pages:1-5 ; date:12.2022
BMC neurology ; 22, Heft 1 (12.2.2022), 1-5, 12.2022
- Urheber
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Durand, Christelle M.
Angelini, Chloé
Michaud, Vincent
Delleci, Claire
Coupry, Isabelle
Goizet, Cyril
Trimouille, Aurelien
- Beteiligte Personen und Organisationen
-
SpringerLink (Online service)
- DOI
-
10.1186/s12883-022-02553-0
- URN
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urn:nbn:de:101:1-2022051819141210912058
- Rechteinformation
-
Open Access; Der Zugriff auf das Objekt ist unbeschränkt möglich.
- Letzte Aktualisierung
- 15.08.2025, 07:21 MESZ
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Beteiligte
- Durand, Christelle M.
- Angelini, Chloé
- Michaud, Vincent
- Delleci, Claire
- Coupry, Isabelle
- Goizet, Cyril
- Trimouille, Aurelien
- SpringerLink (Online service)
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