Correction to: Missense mutations in ITPR1 cause autosomal dominant congenital nonprogressive spinocerebellar ataxia
- 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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Correction to: Missense mutations in ITPR1 cause autosomal dominant congenital nonprogressive spinocerebellar ataxia ; volume:17 ; number:1 ; day:29 ; month:3 ; year:2022 ; pages:1 ; date:12.2022
Orphanet journal of rare diseases ; 17, Heft 1 (29.3.2022), 1, 12.2022
- Urheber
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Huang, Lijia
Warman-Chardon, Jodi
Carter, Melissa T.
Friend, Kathie L.
Dudding, Tracy E.
Schwartzentruber, Jeremy
Zou, Ruobing
Schofield, Peter W.
Douglas, Stuart
Bulman, Dennis E.
Boycott, Kym M.
- Beteiligte Personen und Organisationen
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SpringerLink (Online service)
- DOI
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10.1186/s13023-022-02297-7
- URN
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urn:nbn:de:101:1-2022061812022592653211
- Rechteinformation
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Open Access; Der Zugriff auf das Objekt ist unbeschränkt möglich.
- Letzte Aktualisierung
- 15.08.2025, 05:27 UTC
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Beteiligte
- Huang, Lijia
- Warman-Chardon, Jodi
- Carter, Melissa T.
- Friend, Kathie L.
- Dudding, Tracy E.
- Schwartzentruber, Jeremy
- Zou, Ruobing
- Schofield, Peter W.
- Douglas, Stuart
- Bulman, Dennis E.
- Boycott, Kym M.
- SpringerLink (Online service)
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