SCA12 Spinocerebellar Ataxia Type 12 , CAG Repeats
Detection of abnormal CAG repeats in the ATXN2 gene supports diagnosis of spinocerebellar ataxia type twelve. It assists in confirming hereditary ataxia. Used in family screening.
SCA12 Spinocerebellar Ataxia Type 12 , CAG Repeats
SCA12 Spinocerebellar Ataxia Type 12 , CAG Repeats
