Correction to: Missense mutations in ITPR1 cause autosomal dominant congenital nonprogressive spinocerebellar ataxia

to related objects

Location: Deutsche Nationalbibliothek Frankfurt am Main

ISSN: 1750-1172

Extent: Online-Ressource

Language: Englisch

Notes: online resource.

Bibliographic citation: 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

Creator: 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.

Contributor: SpringerLink (Online service)

DOI: 10.1186/s13023-022-02297-7

URN: urn:nbn:de:101:1-2022061812022592653211

Rights: Open Access; Der Zugriff auf das Objekt ist unbeschränkt möglich.

Last update: 15.08.2025, 7:27 AM CEST

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Associated

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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Correction to: Missense mutations in ITPR1 cause autosomal dominant congenital nonprogressive spinocerebellar ataxia

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Other Objects (12)

Missense mutations in ITPR1 cause autosomal dominant congenital nonprogressive spinocerebellar ataxia

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A Cysteinyl-tRNA Synthetase Mutation Causes Novel Autosomal-Dominant Inheritance of a Parkinsonism/Spinocerebellar-Ataxia Complex

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A Cysteinyl-tRNA Synthetase Mutation Causes Novel Autosomal-Dominant Inheritance of a Parkinsonism/Spinocerebellar-Ataxia Complex

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