A Homozygous RAB3GAP1:c.743delC Mutation in Rottweilers with Neuronal Vacuolation and Spinocerebellar Degeneration

BACKGROUND: A variety of presumed hereditary, neurologic diseases have been reported in young Rottweilers. Overlapping ages of onset and clinical signs have made antemortem diagnosis difficult. One of these diseases, neuronal vacuolation and spinocerebellar degeneration (NVSD) shares clinical and hi...

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Bibliografische gegevens
Gepubliceerd in:J Vet Intern Med
Hoofdauteurs: Mhlanga‐Mutangadura, T., Johnson, G.S., Ashwini, A., Shelton, G.D., Wennogle, S.A., Johnson, G.C., Kuroki, K., O'Brien, D.P.
Formaat: Artigo
Taal:Inglês
Gepubliceerd in: John Wiley and Sons Inc. 2016
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Online toegang:https://ncbi.nlm.nih.gov/pmc/articles/PMC4913561/
https://ncbi.nlm.nih.gov/pubmed/26968732
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1111/jvim.13921
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