Work

Genomewide SNP assay reveals mutations underlying Parkinson disease

Year: 2007

Type: article

Study design: Observational Study

Source: Human Mutation

DOI: 10.1002/humu.20626

Authors: Javier Simon-Sanchez, Sonja Scholz, Maria del Mar Matarin, Hon-Chung Fung, Dena Hernandez, J Raphael Gibbs, Angela Britton, John Hardy, Andrew Singleton

Institutions: National Institutes of Health, Consejo Superior de Investigaciones Científicas, Instituto de Biomedicina de Valencia, UCL Queen Square Institute of Neurology, National Institute on Aging

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: Parkinson's UK, National Institutes of Health, National Institute on Aging, National Institute of Neurological Disorders and Stroke

Award: G3327757157

OpenAlex ID: W2019152017

FWCI: 4.298

Cites: 18

Cited by: 63

Related to: 10