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1 Ergebnisse
1
De Novo and Dominantly Inherited SPTAN1 Mutations Cause Spa..:
Van de Vondel, Liedewei
;
De Winter, Jonathan
;
Beijer, Danique
...
Movement Disorders. 37 (2022) 6 - p. 1175-1186 , 2022
Link:
https://doi.org/10.1002/mds.28959
RT Journal T1
De Novo and Dominantly Inherited SPTAN1 Mutations Cause Spastic Paraplegia and Cerebellar Ataxia
UL https://suche.suub.uni-bremen.de/peid=cr-10.1002_mds.28959&Exemplar=1&LAN=DE A1 Van de Vondel, Liedewei A1 De Winter, Jonathan A1 Beijer, Danique A1 Coarelli, Giulia A1 Wayand, Melanie A1 Palvadeau, Robin A1 Pauly, Martje G. A1 Klein, Katrin A1 Rautenberg, Maren A1 Guillot‐Noël, Léna A1 Deconinck, Tine A1 Vural, Atay A1 Ertan, Sibel A1 Dogu, Okan A1 Uysal, Hilmi A1 Brankovic, Vesna A1 Herzog, Rebecca A1 Brice, Alexis A1 Durr, Alexandra A1 Klebe, Stephan A1 Stock, Friedrich A1 Bischoff, Almut Turid A1 Rattay, Tim W. A1 Sobrido, María‐Jesús A1 De Michele, Giovanna A1 De Jonghe, Peter A1 Klopstock, Thomas A1 Lohmann, Katja A1 Zanni, Ginevra A1 Santorelli, Filippo M. PB Wiley YR 2022 SN 0885-3185 SN 1531-8257 JF Movement Disorders VO 37 IS 6 SP 1175 OP 1186 LK http://dx.doi.org/https://doi.org/10.1002/mds.28959 DO https://doi.org/10.1002/mds.28959 SF ELIB - SuUB Bremen
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