Work

Frequency of the LRRK2 G2019S Mutation in Siblings with Parkinson’s Disease

Year: 2007

Type: article

Study design: Observational Study

Source: Neurodegenerative Diseases

DOI: 10.1159/000101844

Authors: Suzanne Lesage, Laurence Leclere, Ebba Lohmann, Michel Borg, Merle Ruberg, Alexandra Dürr, Alexis Brice

Institutions: Inserm, Assistance Publique – Hôpitaux de Paris, Pitié-Salpêtrière Hospital, Université Pierre-et-Marie-Curie, Physiopathologie des Comportements, Centre Hospitalier Universitaire de Nice

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: W2062694658

FWCI: 1.151

Cites: 27

Cited by: 15

Related to: 10