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Detects mutations in genes associated with spinocerebellar ataxia types 1, 2, and 3.

8,505 THB

Detects mutations in genes associated with spinocerebellar ataxia types 1, 2, and 3.

16,739 THB

Detects mutations in the SCA6 gene, linked to spinocerebellar ataxia type 6.

6,900 THB

Detects mutations in genes associated with types 6, 7, and 12 spinocerebellar ataxia.

10,427 THB

Detects mutations in the ATXN7 gene, responsible for spinocerebellar ataxia type 7.

5,865 THB

Detects mutations in the SURF1 gene, associated with Leigh syndrome.

18,620 THB

Detects mutations in the alpha-globin gene, used to diagnose alpha thalassemia.

4,375 THB

Detects mutations in the beta-globin gene, used for diagnosing beta thalassemia.

7,015 THB

Detects MTHFR mutations, used to assess risk for thrombophilia.

3,250 THB

Detects TSI antibodies to diagnose Graves’ disease, an autoimmune thyroid disorder.

26,928 THB

Detects chromosomal deletions associated with DiGeorge syndrome, a genetic disorder.

8,505 THB

Carrier screening for common genetic conditions using next-generation sequencing and additional molecular methods.

35,840 THB

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