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Wilson Disease (ATP7B gene sequencing)

Neurogenetics

Test Code: WILATP

Genes: ATP7B (1 genes)

Sample Type: 3 ml peripheral blood in EDTA (purple/pink top) tube

Method: Capture-based target enrichment and Next Generation Sequencing.

Turnaround Time: 10- 14 days

Courier: Ship overnight at room temperature to receive next day. Do not refrigerate or freeze. Maintain specimen at room temperature.

Price: 900

Description:
Wilson disease is a genetic disorder caused by mutations in the ATP7B gene, which impair copper transport and lead to toxic accumulation in hepatocytes, as well as in the liver, brain, and other organs.