SCA-6 (SPINOCEREBELLAR ATAXIA), CACNA1A GENE MUTATION

Spinocerebellar ataxia (SCA) or also known as Spinocerebellar atrophy or Spinocerebellar degeneration, is a progressive, degenerative genetic disease with multiple types. In SCA 6 there is a CAG trinucleotide repeat in chromosome 19p which gets affected which results in abnormal CACNA1A protein.

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  • Report Delivery:
    Sample by Tue 11 am; Report Sat
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