Similar oculomotor phenotypes in episodic ataxia type 2 and spinocerebellar atrophy type 6

Ann N Y Acad Sci. 2001 Oct:942:508-9. doi: 10.1111/j.1749-6632.2001.tb03783.x.

Authors

S H Ying¹, J C Jen, R W Baloh

Affiliation

¹ UCLA Department of Neurology, Los Angeles, California 90095, USA. sying@mednet.ucla.edu

PMID: 11710502
DOI: 10.1111/j.1749-6632.2001.tb03783.x

No abstract available

MeSH terms

Ataxia / genetics
Ataxia / physiopathology*
Calcium Channels / genetics
Eye Movements*
Humans
Mutation
Phenotype
Reflex, Vestibulo-Ocular
Spinocerebellar Ataxias / genetics
Spinocerebellar Ataxias / physiopathology*

Substances

CACNA1A protein, human
Calcium Channels