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SCA type 1,2,3,6,7 (Spinocerebellar ataxia)
SKU: MD-NLB141 Categories: , , , , , , , , , , Tags: , , , , , , ,

In Stock

SCA type 1,2,3,6,7 (Spinocerebellar ataxia)

฿15,913.00

Additional information

Also Known As

Spinocerebellar Ataxia Genetic Test, SCA Panel
Specimen

EDTA whole blood 6 ml (minimum 3 ml)
Turnaround Time

30 Days
Test Code

MD-NLB141
Test Type

Special
Related Tests

Ataxia Panel, Whole Exome Sequencing

A genetic test that detects mutations in the genes associated with spinocerebellar ataxia (SCA), a group of inherited neurodegenerative disorders that affect coordination and balance.

Product tags: Coordination Problems, Genetic Disorders, Muscle Weakness, Neurodegenerative Diseases, None, SCA Panel, Slurred Speech, Spinocerebellar Ataxia Genetic Test
Diseases: Genetic Disorders, Neurodegenerative Diseases
Symptoms: Coordination Problems, Muscle Weakness, Slurred Speech
Habits: None
Age Groups: All Ages
Specimens: EDTA Whole Blood
Diagnostic Methods: DNA Sequencing, PCR
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Description

A genetic test that detects mutations in the genes associated with spinocerebellar ataxia (SCA), a group of inherited neurodegenerative disorders that affect coordination and balance.

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

Spinocerebellar Ataxia Genetic Test, SCA Panel
Specimen

EDTA whole blood 6 ml (minimum 3 ml)
Turnaround Time

30 Days
Test Code

MD-NLB141
Test Type

Special
Related Tests

Ataxia Panel, Whole Exome Sequencing

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