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Publication
PropertyValue
Working Groups Klopstock
SubprojectNone
Open AccessOpen Access Yes
Publication TypeJournal Article
Peer ReviewedYes
PMIDPubMed ID 35150594
DOIDOI 10.1002/mds.28959
Publication Year2022
TitleDe Novo and Dominantly Inherited SPTAN1 Mutations Cause Spastic Paraplegia and Cerebellar Ataxia.
JournalMovement disorders : official journal of the Movement Disorder Society
ISSN0885-3185
ESSN1531-8257
URL https://www.ncbi.nlm.nih.gov/pubmed/?term=35150594%5Buid%5D
Pages1175-1186
Issue6
Volume37
Journal AbbreviationMov Disord
AuthorsVan de Vondel L, De Winter J, Beijer D, Coarelli G, Wayand M, Palvadeau R, Pauly MG, Klein K, Rautenberg M, Guillot-Noël L, Deconinck T, Vural A, Ertan S, Dogu O, Uysal H, Brankovic V, Herzog R, Brice A, Durr A, Klebe S, Stock F, Bischoff AT, Rattay TW, Sobrido MJ, De Michele G, De Jonghe P, Klopstock T, Lohmann K, Zanni G, Santorelli FM, Timmerman V, Haack TB, Züchner S, Schüle R, Stevanin G, Synofzik M, Basak AN, Baets J
First AuthorVan de Vondel L
Last AuthorBaets J