Spinocerebellar Ataxia (Beagle)
Body function: Muscle & Neurological
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SPTBN2-related spinocerebellar ataxia is a genetic condition caused by a mutation in the SPTBN2 gene. It is a neurological disorder that causes a severe lack of coordination. This condition is inherited in the autosomal recessive fashion, meaning both parents must be carriers of the mutation for a litter to be affected.
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