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Wilson Disease Mutation
SKU: MD-NLB380 Categories: , , , , , , , , Tags: , , , ,

In Stock

Wilson Disease Mutation

฿32,400.00

Additional information

Also Known As

Wilson's Disease Genetic Test
Specimen

EDTA whole blood 6-10 ml
Turnaround Time

2 months
Test Code

MD-NLB380
Test Type

Special
Related Tests

Liver Panel

Identifies mutations associated with Wilson disease, a genetic disorder affecting copper metabolism.

Product tags: Family History, Genetic Disorders, Liver Dysfunction, Neurological Symptoms, Wilson's Disease Genetic Test
Diseases: Genetic Disorders
Symptoms: Liver Dysfunction, Neurological Symptoms
Habits: Family History
Age Groups: All Ages
Specimens: Blood
Diagnostic Methods: DHPLC, Direct Sequencing
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Description

Identifies mutations associated with Wilson disease, a genetic disorder affecting copper metabolism.

This lab test includes home sample collection via a provided kit or by a clinician, and you'll receive a comprehensive physical health report with your results.

Additional information

Also Known As

Wilson's Disease Genetic Test
Specimen

EDTA whole blood 6-10 ml
Turnaround Time

2 months
Test Code

MD-NLB380
Test Type

Special
Related Tests

Liver Panel

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