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Dystonia in ATP synthase defects: Reconnecting mitochondria and dopamine.
Mov. Disord. 39, 29-35 (2023)
Publication type
Article: Journal article
Document type
Scientific Article
Keywords
Atp Synthase ; Dystonia ; Mitochondrial Diseases ; Movement Disorder; Movement-disorders; Alpha-synuclein; Mutation; Gene; Dna; Disease
ISSN (print) / ISBN
0885-3185
e-ISSN
1531-8257
Journal
Movement Disorders
Quellenangaben
Volume: 39,
Issue: 1,
Pages: 29-35
Publisher
Wiley
Publishing Place
111 River St, Hoboken 07030-5774, Nj Usa
Non-patent literature
Publications
Reviewing status
Peer reviewed
Institute(s)
Institute of Neurogenomics (ING)
Grants
Projekt DEAL
Italian Ministry of Health and Fondazione Mariani
Technical University of Munich-Institute for Advanced Study
Laender
Free State of Bavaria under Excellence Strategy of Federal Government
Federal Ministry of Education and Research (BMBF)
European Joint Programme on Rare Diseases (EJP RD Joint Transnational)
German Federal Ministry of Education and Research (BMBF, Bonn, Germany)
German Research Foundation
European Joint Programme on Rare Diseases
Italian Ministry of Health and Fondazione Mariani
Technical University of Munich-Institute for Advanced Study
Laender
Free State of Bavaria under Excellence Strategy of Federal Government
Federal Ministry of Education and Research (BMBF)
European Joint Programme on Rare Diseases (EJP RD Joint Transnational)
German Federal Ministry of Education and Research (BMBF, Bonn, Germany)
German Research Foundation
European Joint Programme on Rare Diseases