| EX1516 MITOCHONDRIAL MUTATION DETECTION COMPREHENSIVE PANEL |
| 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, Sequencing |
| Comment: |
Samples received on holidays will be reported in the next schedule/next working day. |
| Report: |
Contact us to know the TAT. |
| Usage: |
This test is useful for elucidation of mitochondrial mutations linked to various mitochondrial diseases such as mitochondrial myopathy, MELAS, MERFF, LHON, LEIGH syndrome, Deafness, etc. |
| Doctor Specialty: |
Neurologist, Pediatrician |
| Disease: |
Neurological disorders, Genetic diseases |
| Components: |
*ND1 *ND4 *ND5 *ND6 *TL1 *MCTYB1 *ATP6 *ATP8 |
| Courier Charges: |
|
| 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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