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Ataxia-ocular apraxia 2 (AOA2, sequence analysis of SETX gene)
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Specimen Requirements

Descriptive Volume /
Concentration 1
Container Transport
viability (days) 2
DNA ≥ 100 µL [50 ng/µL] Eppendorf Safe-lock Room temp. n/a
Peripheral blood ≥ 3 mL EDTA Room temp. 5
1 When it is not possible to collect the minimum volume for the test, please contact CGC Genetics
2 Maximum shipping time to ensure sample quality

Turnaround Time (Days)

- 60

CPT Codes

- 81406


- Rare diseases, Neurology / Neuropediatrics, Ophthalmology, Pediatrics

CGC Reference

- 1892

Associated Tests

Amyotrophic lateral sclerosis 4, juvenile (sequence analysis of SETX gene)
Amyotrophic lateral sclerosis (deletion/duplication analysis on SETX gene)
Recessives ataxias (deletion/duplication analysis on SETX, APTX and FXN genes)
Amyotrophic lateral sclerosis/motor neuron disease (WES based NGS panel of 29 genes, including CNV analysis)