Dystonia in ATP Synthase Defects: Reconnecting Mitochondria and Dopamine

Elisabetta Indelicato, Sylvia Boesch, Niccolo' E. Mencacci, Daniele Ghezzi, Holger Prokisch, Juliane Winkelmann, Michael Zech*

*Corresponding author for this work

Research output: Contribution to journalArticlepeer-review

2 Scopus citations
Original languageEnglish (US)
Pages (from-to)29-35
Number of pages7
JournalMovement Disorders
Volume39
Issue number1
DOIs
StatePublished - Jan 2024

Funding

E.I. is supported by the European Joint Programme on Rare Diseases (EJP‐RD WP17 research mobility fellowship). J.W. and M.Z. receive research support from the German Research Foundation (DFG 458949627; WI 1820/14‐1; ZE 1213/2‐1). H.P. acknowledges grant support from the German Federal Ministry of Education and Research (BMBF, Bonn, Germany) awarded to the German Network for Mitochondrial Disorders (mitoNET, 01GM1906A). M.Z. acknowledges grant support by the European Joint Programme on Rare Diseases (EJP RD Joint Transnational Call 2022), and the German Federal Ministry of Education and Research (BMBF, Bonn, Germany), awarded to the project PreDYT (Predictive biomarkers in dystonia, 01GM2302), by the Federal Ministry of Education and Research (BMBF) and the Free State of Bavaria under the Excellence Strategy of the Federal Government and the Länder, as well as by the Technical University of Munich‐Institute for Advanced Study. D.G. acknowledges grant support from the Italian Ministry of Health and Fondazione Mariani. Open Access funding enabled and organized by Projekt DEAL. E.I. is supported by the European Joint Programme on Rare Diseases (EJP-RD WP17 research mobility fellowship). J.W. and M.Z. receive research support from the German Research Foundation (DFG 458949627; WI 1820/14-1; ZE 1213/2-1). H.P. acknowledges grant support from the German Federal Ministry of Education and Research (BMBF, Bonn, Germany) awarded to the German Network for Mitochondrial Disorders (mitoNET, 01GM1906A). M.Z. acknowledges grant support by the European Joint Programme on Rare Diseases (EJP RD Joint Transnational Call 2022), and the German Federal Ministry of Education and Research (BMBF, Bonn, Germany), awarded to the project PreDYT (Predictive biomarkers in dystonia, 01GM2302), by the Federal Ministry of Education and Research (BMBF) and the Free State of Bavaria under the Excellence Strategy of the Federal Government and the Länder, as well as by the Technical University of Munich-Institute for Advanced Study. D.G. acknowledges grant support from the Italian Ministry of Health and Fondazione Mariani. Open Access funding enabled and organized by Projekt DEAL.

Keywords

  • ATP synthase
  • dystonia
  • mitochondrial diseases
  • movement disorder

ASJC Scopus subject areas

  • Neurology
  • Clinical Neurology

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