| 1 | RNF170, SNAX1 |
| A mutation in the RNF170 gene causes autosomal dominant sensory ataxia. | |
| Valdmanis PN, Dupré N, Lachance M, Stochmanski SJ, Belzil VV, Dion PA, Thiffault I, Brais B, Weston L, Saint-Amant L, Samuels ME, Rouleau GA. | |
| Brain 134(Pt 2):602-7. Epub 2010 Nov 28. 2011 | |
| 2 | SNAX1 |
| A novel neurodegenerative disease characterised by posterior column ataxia and pyramidal tract involvement maps to chromosome 8p12-8q12.1. | |
| Valdmanis PN, Simoes Lopes AA, Gros-Louis F, Stewart JD, Rouleau GA, Dupre N. | |
| J Med Genet 41(8):634-9. No abstract available. 2004 | |