Work

Frequency of spinocerebellar ataxia type 1, dentatorubropallidoluysian atrophy, and Machado-Joseph disease mutations in a large group of spinocerebellar ataxia patients

Year: 1996

Type: article

Study design: Observational Study

Source: Neurology

DOI: 10.1212/wnl.46.1.214

Institutions: McGill University, University of Toronto, Universidade do Porto, Hôtel-Dieu de Montréal, Universidade Estadual de Campinas (UNICAMP), All India Institute of Medical Sciences, Johns Hopkins University, Harvard University, Queen Elizabeth II Health Sciences Centre

Language: English

Topic: Genetic Neurodegenerative Diseases

Subfield: Cellular and Molecular Neuroscience

Field: Neuroscience

Domain: Life Sciences

SDG: Good health and well-being

Open Access status: closed

Funders: U.S. Public Health Service, National Institute of Neurological Disorders and Stroke

Awards: IDENTIFICATION OF THE MACHADO JOSEPH DISEASE GENE, G9000307572

OpenAlex ID: W2015419243

FWCI: 4.379

Cites: 38

Cited by: 105

Related to: 10