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WILATP

Wilson Disease (ATP7B gene sequencing)

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.

Neurogenetics
Sample: 3 ml peripheral blood in EDTA (purple/pink top) tube
TAT: 10- 14 days
Price:
Genes: 1 genes
Details