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Screens for genetic variations associated with brain diseases using SNP array and polygenic risk scoring.

22,626 THB

Detects deletions in exon 7 of the SMN1 gene, responsible for spinal muscular atrophy (SMA).

11,235 THB

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

18,620 THB

Detects antibodies against voltage-gated calcium channels, used in diagnosing Lambert-Eaton myasthenic syndrome (LEMS).

73,600 THB

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