Corrigendum to "Expanding the phenotype of RBCK1-associated polyglucosan body myopathy type 1".

Journal

Molecular genetics and metabolism reports
ISSN: 2214-4269
Titre abrégé: Mol Genet Metab Rep
Pays: United States
ID NLM: 101624422

Informations de publication

Date de publication:
Mar 2024
Historique:
medline: 12 3 2024
pubmed: 12 3 2024
entrez: 12 3 2024
Statut: epublish

Résumé

[This corrects the article DOI: 10.1016/j.ymgmr.2023.101031.].

Identifiants

DOI: 10.1016/j.ymgmr.2023.101039 PMID: 38469095 PMC: PMC10926214
pubmed: 38469095
doi: 10.1016/j.ymgmr.2023.101039
pii: S2214-4269(23)00085-X
pmc: PMC10926214
doi:

Types de publication

Published Erratum

Langues

eng

Pagination

101039

Commentaires et corrections

Type : ErratumFor

Informations de copyright

© 2023 The Author(s).

Auteurs

Manuel Pühringer (M)

Department of Paediatrics and Adolescent Medicine, Kepler University Hospital, Linz, Austria.

Astrid Eisenkölbl (A)

Department of Paediatrics and Adolescent Medicine, Kepler University Hospital, Linz, Austria.

Gudrun Gröppel (G)

Department of Paediatrics and Adolescent Medicine, Kepler University Hospital, Linz, Austria.
Department of Neurology, Kepler University Hospital, Linz, Austria.

Classifications MeSH