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Publication
Property
Value
Working Groups
Klopstock
Subproject
None
Open Access
Yes
Publication Type
Journal Article
Peer Reviewed
Yes
PMID
33134520
DOI
10.1212/NXG.0000000000000525
Publication Year
2020
Title
Biotinidase deficiency: A treatable cause of hereditary spastic paraparesis.
Journal
Neurology. Genetics
ISSN
2376-7839
ESSN
2376-7839
URL
https://www.ncbi.nlm.nih.gov/pubmed/?term=33134520%5Buid%5D
Pages
e525
Issue
6
Volume
6
Journal Abbreviation
Neurol Genet
Authors
Radelfahr F, Riedhammer KM, Keidel LF, Gramer G, Meitinger T, Klopstock T, Wagner M
First Author
Radelfahr F
Last Author
Wagner M
Scholia
Wikidata-based representation at Scholia
External Resources
Q101146153
https://www.wikidata.org/wiki/Q101146153
Wikidata ID