Reference List
| Author | Title | Journal | Year | Vol(Iss)Pg | PubMed ID | Abstract |
|---|---|---|---|---|---|---|
| A truncated retrotransposon disrupts the GRM1 coding sequence in Coton de Tulear dogs with Bandera's neonatal ataxia. | J Vet Intern Med | 2011 | 25:267-72, 2011. | 21281350 | Show | |
| Neonatal cerebellar ataxia in Coton de Tulear dogs | Journal of Veterinary Internal Medicine | 2002 | 16:680-9, 2002. | 12465765 | Show | |
| Progressive ataxia and seizures in a Cocker Spaniel: a new type of neurodegenerative disease with novel intra-neuronal inclusions | New Zealand Veterinary Journal | 2002 | 50:203-206, 2002. | |||
| A SEL1L Mutation Links a Canine Progressive Early-Onset Cerebellar Ataxia to the Endoplasmic Reticulum-Associated Protein Degradation (ERAD) Machinery. | PLoS Genet | 2012 | 8:e1002759, 2012. | 22719266 | Show | |
| [Cerebellar ataxia in a Finnish hurrier] Ett fall av cerebellar ataxi hos finsk stövare (Swedish) | Suomen Eläinlääkärilehti | 1971 | 77:135–138, 1971. | |||
| Changes in mutation frequency of eight Mendelian inherited disorders in eight pedigree dog populations following introduction of a commercial DNA test. | PLoS One | 2019 | 14:e0209864, 2019. | 30650096 | Show | |
| [Correction to] Mutations in CAPN1 Cause Autosomal-Recessive Hereditary Spastic Paraplegia. | American Journal of Human Genetics | 2016 | 98:1271, 2016. | 27259058 | Show | |
| Mutations in CAPN1 Cause Autosomal-Recessive Hereditary Spastic Paraplegia. | Am J Hum Genet | 2016 | 98:1038-1046, 2016. | 27153400 | Show | |
| Defects in the CAPN1 Gene Result in Alterations in Cerebellar Development and Cerebellar Ataxia in Mice and Humans. | Cell Reports | 2016 | 16:79-91, 2016. | 27320912 | Show | |
| Hereditary ataxia in Jack Russell terriers in the UK. | Vet Rec | 2014 | 174:258, 2014. | 24736826 | Show |