View publication

↩ Back to all publications
Publication
PropertyValue
Working Groups Klopstock
SubprojectNone
Open AccessOpen Access Yes
Publication TypeJournal Article
Peer ReviewedYes
PMIDPubMed ID 33134520
DOIDOI 10.1212/NXG.0000000000000525
Publication Year2020
TitleBiotinidase deficiency: A treatable cause of hereditary spastic paraparesis. Wikidata
JournalNeurology. Genetics
ISSN2376-7839
ESSN2376-7839
URL https://www.ncbi.nlm.nih.gov/pubmed/?term=33134520%5Buid%5D
Pagese525
Issue6
Volume6
Journal AbbreviationNeurol Genet
AuthorsRadelfahr F, Riedhammer KM, Keidel LF, Gramer G, Meitinger T, Klopstock T, Wagner M
First AuthorRadelfahr F
Last AuthorWagner M
ScholiaScholia Wikidata-based representation at Scholia

 External Resources

 Q101146153  Wikidata ID