Genetic Tests for Rare Neurodiseases (English version)

8 Aug, 2016
Spinocerebellar atrophy is a hereditary disease mainly caused by genetic mutations. For a person with dominant genes of spinocerebellar atrophy, there is a 50% chance that his / her offspring will inherit spinocerebellar atrophy as well. How can we know if we carry dominant genes of spinocerebellar atrophy? A genetic test can help. 

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