A Novel NPTX1 de novo Variant in a Late-Onset Ataxia Patient
Mov Disord
.
2022 Jun;37(6):1319-1321.
doi: 10.1002/mds.28985.
Epub 2022 Mar 14.
Authors
Jonas Deppe
1
,
Natalie Deininger
2
,
Paul Lingor
1
,
Tobias B Haack
2
3
,
Bernhard Haslinger
1
,
Marcus Deschauer
1
Affiliations
1
Department of Neurology, School of Medicine, Technical University of Munich, Munich, Germany.
2
Institute of Medical Genetics and Applied Genomics, University of Tübingen, Tübingen, Germany.
3
Centre for Rare Diseases, University of Tübingen, Tübingen, Germany.
PMID:
35285082
DOI:
10.1002/mds.28985
No abstract available
Publication types
Letter
Research Support, Non-U.S. Gov't
MeSH terms
Ataxia / genetics
Cerebellar Ataxia*
Humans