| EX1031 HUNTINGTON DISEASE MUTATION DETECTION |
| Specimen: |
4 mL (2 mL min.) whole blood in 1 Lavender top (EDTA) tube. Ship refrigerated. DO NOT FREEZE. |
| Stability: |
| Room |
Refrigerated |
Frozen |
| 6 hrs |
1 week |
NA |
|
| Method: |
PCR Fragment analysis |
| Comment: |
|
| Report: |
Contact us to know the TAT. |
| Usage: |
Huntington’s disease is a neurodegenerative genetic disorder that affects muscle coordination and leads to mental decline and behavioral symptoms. Less than 26 repeats of nucleotide CAG is normal, 40 or more lead to symptoms while between 26-40 repeats is intermediate. |
| Doctor Specialty: |
Neurologist |
| Disease: |
Disorders of Nervous System |
| Components: |
|
| Courier Charges: |
0.00 |
| Home Collection: |
Available (*T&C Apply) |
| Department: |
MOLECULAR DIAGNOSTICS |
| Pre Test Information: |
A duly filled Genomics Clinical Information Requisition Form is mandatory. |
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