Eye movement abnormalities correlate with genotype in autosomal dominant cerebellar ataxia type I
Year: 1998
Type: review
Study design: Observational Study
Source: Annals of Neurology
Language: English
Subfield: Cellular and Molecular Neuroscience
Field: Neuroscience
Domain: Life Sciences
Open Access status: closed
OpenAlex ID: W2154590865
