Work

Clinical and genetic analysis of a Tunisian family with autosomal dominant cerebellar ataxia type 1linked to the SCA2 locus

Year: 1994

Type: article

Study design: Observational Study

Source: Neurology

DOI: 10.1212/wnl.44.8.1423

Authors: S. Belal, G. Cancel, G. Stevanin, F. Hentati, C. Khati, C. Ben Hamida, G. Auburger, Y. Agid, M. Ben Hamida, A. Brice

Institutions: Inserm, Düsseldorf University Hospital, Pitié-Salpêtrière Hospital, National Institute of Neurology Mongi-Ben Hamida, Physiopathologie des Comportements

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

OpenAlex ID: W2116758780

FWCI: 2.97

Cites:

Cited by: 54

Related to: 10