De Novo and Dominantly Inherited SPTAN1 Mutations Cause Spastic Paraplegia and Cerebellar Ataxia is a research paper published in Movement Disorders (2022). On theSindex it has a DataRank of 0. It has been cited 26 times.
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Deutsche Forschungsgemeinschaft
Grant: 418081722
Deutsche Forschungsgemeinschaft
Grant: 433158657
Deutsche Forschungsgemeinschaft
Grant: 441409627
Eberhard Karls Universität Tübingen
Grant: 386‐0‐0
Fonds Wetenschappelijk Onderzoek
Grant: 11F0921N
Fonds Wetenschappelijk Onderzoek
Grant: 1805021
Horizon 2020 Framework Programme
Grant: 779257
Solving the unsolved Rare Diseases
National Institutes of Health
Grant: 5R01NS072248
Universiteit Antwerpen
Grant: FFB210049
NINDS NIH HHS
Grant: R01 NS072248
NINDS NIH HHS
Grant: R01 NS105755
European Commission
Grant: 825575
European Joint Programme on Rare Diseases
National Institutes of Health
Grant: 5R01NS105755-03
Genomic Studies in Charcot-Marie-Tooth Disease
National Institutes of Health
Grant: 5R01NS072248-10
GENOME STUDIES IN HEREDITARY SPASTIC PARAPLEGIA - beyond the exome
Deutsche Forschungsgemeinschaft
Grant: unidentified
unidentified
Damp Stiftung
Association Belge contre les Maladies Neuro-Musculaires
FWCI
2.30
Citation Percentile
0.9%
Citation Trend
Fields of Study
MeSH Terms
Keywords
Sustainable Development Goals