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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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Detaylı Bibliyografya
Yayımlandı:J Vet Intern Med
Asıl Yazarlar: Mhlanga‐Mutangadura, T., Johnson, G.S., Ashwini, A., Shelton, G.D., Wennogle, S.A., Johnson, G.C., Kuroki, K., O'Brien, D.P.
Materyal Türü: Artigo
Dil:Inglês
Baskı/Yayın Bilgisi: John Wiley and Sons Inc. 2016
Konular:
Online Erişim: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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