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Publication
PropertyValue
Working Groups Klopstock
SubprojectNone
Open AccessOpen Access Yes
Publication TypeJournal Article
Peer ReviewedYes
PMIDPubMed ID 35945620
DOIDOI 10.1186/s13023-022-02453-z
Publication Year2022
TitleVitamin B12 in Leber hereditary optic neuropathy mutation carriers: a prospective cohort study.
JournalOrphanet journal of rare diseases
ESSN1750-1172
URL https://www.ncbi.nlm.nih.gov/pubmed/?term=35945620%5Buid%5D
Pages310
Issue1
Volume17
Journal AbbreviationOrphanet J Rare Dis
AuthorsZibold J, von Livonius B, Kolarova H, Rudolph G, Priglinger CS, Klopstock T, Catarino CB
First AuthorZibold J
Last AuthorCatarino CB