A Wide Variety of Mutations in the Parkin Gene Are Responsible for Autosomal Recessive Parkinsonism in Europe
Year: 1999
Type: article
Study design: Observational Study
Source: Human Molecular Genetics
DOI: 10.1093/hmg/8.4.567
Authors: N. Abbas, C. B. Lucking, S. Ricard, A. Durr, V. Bonifati, G. De Michele, S. Bouley, J. R. Vaughan, T. Gasser, R. Marconi, E. Broussolle, C. Brefel-Courbon, B. S. Harhangi, B. A. Oostra, E. Fabrizio, G. A. Bohme, L. Pradier, N. W. Wood, A. Filla, G. Meco, P. Denefle, Y. Agid, A. Brice, French Parkinson's Disease Genetics Study Group
Institutions: Inserm, Physiopathologie des Comportements, Sapienza University of Rome, University of Naples Federico II, National Hospital for Neurology and Neurosurgery, UCL Queen Square Institute of Neurology, Ludwig-Maximilians-Universität München, Ospedale Misericordia - Grosseto, Hôpital Pierre Wertheimer, Centre Hospitalier Universitaire de Toulouse, Erasmus MC, Erasmus University Rotterdam, Université Pierre-et-Marie-Curie
Language: English
Subfield: Neurology
Field: Medicine
Domain: Health Sciences
Open Access status: closed
OpenAlex ID: W2117335809