Test Code: WILATP

Wilson Disease (ATP7B gene sequencing)

Neurogenetics
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.
Sample Type
3 ml peripheral blood in EDTA (purple/pink top) tube
Turnaround Time
10- 14 days days
Courier Requirements
Ship overnight at room temperature to receive next day. Do not refrigerate or freeze. Maintain specimen at room temperature.
Pricing

Genes Analyzed

1 genes
ATP7B

Methodology

Capture-based target enrichment and Next Generation Sequencing.

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