OpenAlex
PricingAboutJobs
Log inGet started
Work

Eye movement abnormalities correlate with genotype in autosomal dominant cerebellar ataxia type I

HTML

Year: 1998
Type: review
Study design: Observational Study
Source: Annals of Neurology
DOI: 10.1002/ana.410430306
Authors: Sophie Rivaud‐Pechoux, Alexandra Dürr, Bertrand Gaymard, Géaraldine Cancel, Christoph J. Ploner, Yves Agid, Alexis Brice, Charles Pierrot‐Deseilligny
Institutions: Inserm, Physiopathologie des Comportements, Charité – Universitätsmedizin Berlin, Stiftung Charité
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: W2154590865
FWCI: 0.551
Cites: 32
Cited by: 88
Related to: 10
OpenAlex
Nonprofit
Open DataOpen Data
Open Source
Product
Search
Compare
Pricing
Repositories
Unpaywall
Unsub
Developers
API docs
Data snapshot
Status
Source code
Organization
About
Team
Testimonials
Brand
Jobs
Community
Help center
Contact
Events
Blog
Mailing list
Supporters
Legal
Privacy
Accessibility
Terms