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Indelicato, E. ; Romito, L.M.* ; Harrer, P. ; Golfrè Andreasi, N.* ; Colangelo, I.* ; Kopajtich, R. ; Winkelmann, J. ; Prokisch, H. ; Garavaglia, B.* ; Zech, M.

Genome aggregation database version 4-new challenges of variant analysis in movement disorders.

Mov. Disord., DOI: 10.1002/mds.29797 (2024)
Publ. Version/Full Text DOI PMC
Open Access Hybrid
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Publication type Article: Journal article
Document type Scientific Article
Language english
Publication Year 2024
HGF-reported in Year 2024
ISSN (print) / ISBN 0885-3185
e-ISSN 1531-8257
Journal Movement Disorders
Publisher Wiley
Publishing Place 111 River St, Hoboken 07030-5774, Nj Usa
Reviewing status Peer reviewed
Institute(s) Institute of Neurogenomics (ING)
POF-Topic(s) 30205 - Bioengineering and Digital Health
Research field(s) Genetics and Epidemiology
PSP Element(s) G-503200-001
G-503292-001
Grants European Joint Programme on Rare Diseases
German Research Foundation (DFG)
Italian Ministry of Health
German Federal Ministry of Education and Research (BMBF, Bonn, Germany)
European Joint Programme on Rare Diseases (EJP-RD Joint Transnational Call 2022)
Federal Ministry of Education and Research (BMBF)
Free State of Bavaria under the Excellence Strategy of the Federal Government and the Laender
Technical University of Munich-Institute
Else Kroener-Fresenius-Stiftung
Projekt DEAL

European Reference Network for Rare Neurological Diseases (ERN-RND)
DOI 10.1002/mds.29797
WOS ID 001189018900001
Scopus ID 85189093641
PubMed ID 38516945
Erfassungsdatum 2024-05-13
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