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SCA type 7
SKU: MD-NLM995 Categories: , , , , , , , Tags: , , , ,

In Stock

SCA type 7

฿5,865.00

Additional information

Also Known As

Spinocerebellar Ataxia Type 7 Test
Specimen

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

30 Days
Test Code

MD-NLM995
Test Type

Special
Related Tests

Genetic Testing Panel

Detects mutations in the ATXN7 gene, responsible for spinocerebellar ataxia type 7.

Product tags: Coordination Problems, Family History, Neurological Disorders, Spinocerebellar Ataxia Type 7 Test, Vision Loss
Diseases: Neurological Disorders
Symptoms: Coordination Problems, Vision Loss
Habits: Family History
Age Groups: All Ages
Specimens: Blood
Diagnostic Methods: PCR
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Description

Detects mutations in the ATXN7 gene, responsible for spinocerebellar ataxia type 7.

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 Type 7 Test
Specimen

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

30 Days
Test Code

MD-NLM995
Test Type

Special
Related Tests

Genetic Testing Panel

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