Work

EIF4G1 in familial Parkinson's disease: pathogenic mutations or rare benign variants?

Year: 2012

Type: article

Study design: Observational Study

Source: Neurobiology of Aging

DOI: 10.1016/j.neurobiolaging.2012.05.006

Authors: Suzanne Lesage, Christel Condroyer, Stephan Klebe, Ebba Lohmann, Franck Durif, Philippe Damier, François Tison, Mathieu Anheim, Aurélie Honoré, François Viallet, Anne-Marie Bonnet, Anne-Marie Ouvrard-Hernandez, Marie Vidailhet, Alexandra Durr, Alexis Brice

Institutions: Centre National de la Recherche Scientifique, Inserm, Pitié-Salpêtrière Hospital, Institut du Cerveau, Université Pierre-et-Marie-Curie, Universitätsklinikum Würzburg, Centre Hospitalier Universitaire de Clermont-Ferrand, Centre Hospitalier Universitaire de Nantes, Université de Bordeaux, Centre Hospitalier Universitaire de Bordeaux, Institut des Maladies Neurodégénératives, Centre Hospitalier Intercommunal Aix-Pertuis, Centre Hospitalier Universitaire de Grenoble

Language: English

Topic: Parkinson's Disease Mechanisms and Treatments

Subfield: Neurology

Field: Medicine

Domain: Health Sciences

SDG: Good health and well-being

Open Access status: green

Funder: Agence Nationale de la Recherche

Awards: G1432052651, Transfer of misfolded protein as a pathogenetic mechanism in neurodegenerative disease, Identification of new genes causing familial forms of PD

OpenAlex ID: W2063010671

FWCI: 3.957

Cites: 8

Cited by: 41

Related to: 10