Origin of the Mutations in the parkin Gene in Europe: Exon Rearrangements Are Independent Recurrent Events, whereas Point Mutations May Result from Founder Effects
Year: 2001
Type: article
Study design: Observational Study
DOI: 10.1086/318791
Authors: Magali Periquet, Christoph B. Lücking, Jenny R. Vaughan, Vincenzo Bonifati, Alexandra Dürr, Giuseppe De Michele, Martin W. Horstink, Matt Farrer, Sergei N. Illarioshkin, Pierre Pollak, Michel Borg, Christine Brefel-Courbon, Patrice Denefle, Giuseppe Meco, Thomas Gasser, Monique M.B. Breteler, Nick W. Wood, Yves Agid, Alexis Brice
Institutions: Inserm, Pitié-Salpêtrière Hospital, Physiopathologie des Comportements, UCL Queen Square Institute of Neurology, Sapienza University of Rome, University of Naples Federico II, Mayo Clinic, Mayo Clinic in Florida, Research Center of Neurology, Centre Hospitalier Universitaire de Grenoble, Hôpital Pasteur, Sanofi (France), Ludwig-Maximilians-Universität München
Language: English
Subfield: Neurology
Field: Medicine
Domain: Health Sciences
Open Access status: bronze
OpenAlex ID: W2024794315