Reference List
| Author | Title | Journal | Year | Vol(Iss)Pg | PubMed ID | Abstract |
|---|---|---|---|---|---|---|
| Genome-wide mRNA sequencing of a single canine cerebellar cortical degeneration case leads to the identification of a disease associated SPTBN2 mutation. | BMC Genet | 2012 | 13:55, 2012. | 22781464 | Show | |
| Spinocerebellar ataxia in the Italian Spinone dog is associated with an intronic GAA repeat expansion in ITPR1. | Mamm Genome | 2015 | 26:108-17, 2015. | 25354648 | Show | |
| A SINE Insertion in ATP1B2 in Belgian Shepherd Dogs Affected by Spongy Degeneration with Cerebellar Ataxia (SDCA2). | G3 (Bethesda) | 2017 | 7:2729-2737, 2017. | 28620085 | Show | |
| A Missense Variant in <i>SCN8A</i> in Alpine Dachsbracke Dogs Affected by Spinocerebellar Ataxia. | Genes (Basel) | 2019 | 10:, 2019. | 31083464 | Show | |
| Characterisation of canine KCNIP4: A novel gene for cerebellar ataxia identified by whole-genome sequencing two affected Norwegian Buhund dogs. | PLoS Genet | 2020 | 16:e1008527, 2020. | 31999692 | Show | |
| Hereditary ataxia in four related Norwegian Buhunds. | J Am Vet Med Assoc | 2018 | 253:774-780, 2018. | 30179085 | Show | |
| Truncating SLC12A6 variants cause different clinical phenotypes in humans and dogs. | Eur J Hum Genet | 2019 | 27:1561-1568, 2019. | 31160700 | Show |