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Dystonia in ATP synthase defects: Reconnecting mitochondria and dopamine.
Mov. Disord. 39, 29-35 (2023)
Verlagsversion
DOI
PMC
Publikationstyp
Artikel: Journalartikel
Dokumenttyp
Wissenschaftlicher Artikel
Schlagwörter
Atp Synthase ; Dystonia ; Mitochondrial Diseases ; Movement Disorder; Movement-disorders; Alpha-synuclein; Mutation; Gene; Dna; Disease
ISSN (print) / ISBN
0885-3185
e-ISSN
1531-8257
Zeitschrift
Movement Disorders
Quellenangaben
Band: 39,
Heft: 1,
Seiten: 29-35
Verlag
Wiley
Verlagsort
111 River St, Hoboken 07030-5774, Nj Usa
Nichtpatentliteratur
Publikationen
Begutachtungsstatus
Peer reviewed
Institut(e)
Institute of Neurogenomics (ING)
Förderungen
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