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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Detalles Bibliográficos
Autores principales: Mhlanga‐Mutangadura, T., Johnson, G.S., Ashwini, A., Shelton, G.D., Wennogle, S.A., Johnson, G.C., Kuroki, K., O'Brien, D.P.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2016
Materias:
SMALL ANIMAL
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4913561/
https://www.ncbi.nlm.nih.gov/pubmed/26968732
http://dx.doi.org/10.1111/jvim.13921

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4913561/
https://www.ncbi.nlm.nih.gov/pubmed/26968732
http://dx.doi.org/10.1111/jvim.13921

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