Links
[1] http://ghr.nlm.nih.gov/gene/ATXN1
[2] https://disorders.eyes.arizona.edu/disorders/spinocerebellar-ataxia-7
[3] http://omim.org/entry/164500
[4] https://disorders.eyes.arizona.edu/references/maculopathy-and-spinocerebellar-ataxia-type-1-new-association
[5] https://disorders.eyes.arizona.edu/references/novel-maculopathy-patients-spinocerebellar-ataxia-type-1-autofluorescence-findings-and
[6] https://disorders.eyes.arizona.edu/references/rod-cone-dystrophy-spinocerebellar-ataxia-type-1
[7] https://disorders.eyes.arizona.edu/references/autosomal-dominant-cerebellar-ataxia-type-i-oculomotor-abnormalities-families-sca1-sca2
[8] https://disorders.eyes.arizona.edu/references/oculomotor-phenotypes-autosomal-dominant-ataxias
[9] https://disorders.eyes.arizona.edu/references/eye-movement-abnormalities-correlate-genotype-autosomal-dominant-cerebellar-ataxia-type-i
[10] https://disorders.eyes.arizona.edu/references/temporal-retinal-nerve-fiber-loss-patients-spinocerebellar-ataxia-type-1