Work

Absence of NR4A2 exon 1 mutations in 108 families with autosomal dominant Parkinson disease

Year: 2004

Type: article

Study design: Observational Study

Source: Neurology

DOI: 10.1212/01.wnl.0000127496.23198.75

Authors: P. Ibáñez, E. Lohmann, P. Pollak, F. Durif, C. Tranchant, Y. Agid, A. Dürr, A. Brice

Institutions: Inserm, Centre Hospitalier Universitaire de Grenoble, Pitié-Salpêtrière Hospital, Physiopathologie des Comportements

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: closed

Funders: National Institutes of Health, National Institute of Neurological Disorders and Stroke

Awards: Parkin mutations and their functional consequences, G577149390

OpenAlex ID: W1980402099

FWCI: 0.895

Cites: 8

Cited by: 18

Related to: 10