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Truncating SLC12A6 Mutation as a Cause of a Hereditary, Slowly Progressive, Spinocerebellar Ataxia with Severe Central Axonopathy in a Malinois Dog Family. (January 2020)
Record Type:
Journal Article
Title:
Truncating SLC12A6 Mutation as a Cause of a Hereditary, Slowly Progressive, Spinocerebellar Ataxia with Severe Central Axonopathy in a Malinois Dog Family. (January 2020)
Main Title:
Truncating SLC12A6 Mutation as a Cause of a Hereditary, Slowly Progressive, Spinocerebellar Ataxia with Severe Central Axonopathy in a Malinois Dog Family