Yerevan
EN
Lab tests
42-044

Determination of triplet expansion in spinocerebellar ataxia type 2 (in the ATXN2 gene)

Description

An increase in the number of CAG triplet repeats (expansion) in the coding region of the ATX2 gene causes spinocerebellar ataxia type 2, a common autosomal dominant neurological disorder.

Period of execution

Within 12 days. The specified time does not include the day of biomaterial collection

Biomaterial type

  • Venous blood
Total price
21765 ֏
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