Spinocerebellar Ataxia Type 2

TEST CODE MG02840
TEST NAME Spinocerebellar Ataxia Type 2
RELATED GENE ATXN2
SYNONYMOUS ATXN2
OMIM 183090
HEREDITY Autosomal Dominant
CLINICAL AREA Spinocerebellar Ataxia Type 2 is an Autosomal Dominant inherited disease. Mutations in the ATXN2 gene have been associated with the disease.
METHOD Next Generation Sequencing
SAMPLE TYPE Blood with EDTA
QUANTITY 3 mL
TAT 40 DAYS

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