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Screening for DJ-1 mutations in early onset autosomal recessive parkinsonism

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Year: 2003
Type: article
Study design: Observational Study
Source: Neurology
DOI: 10.1212/01.wnl.0000094121.48373.fd
Authors: P. Ibáñez, G. De Michele, V. Bonifati, E. Lohmann, S. Thobois, P. Pollak, Y. Agid, P. Heutink, A. Dürr, A. Brice, the French Parkinson’s Disease Genetics Study Group
Institutions: Inserm, Centre Hospitalier Universitaire de Grenoble, Federico II University Hospital, Pitié-Salpêtrière Hospital, Physiopathologie des Comportements, University of Naples Federico II, Sapienza University of Rome, Erasmus MC
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: Association France Parkinson, National Institutes of Health, National Institute of Neurological Disorders and Stroke
Awards: Parkin mutations and their functional consequences, G577149390
OpenAlex ID: W2053784053
FWCI: 2.368
Cites: 11
Cited by: 38
Related to: 10
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