Spinocerebellar ataxia type 7 (SCA7) is one of several autosomal dominant ataxias characterized by neuronal loss, usually in the cerebellum and brainstem. The cause of SCA7 is a heterozygote mutation of the CAG repeats expansion [5]. Generally, the CAG repeat in SCA7 patients expands from 37 to 460 triplets.
Sample Type - Blood
Reporting Time - Please Call Customer care
Prerequisites - No special preparation required
Price - ₹4000/-
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