Dravet Syndrome
| TEST CODE | MG00860 |
| TEST NAME | Dravet Syndrome |
| RELATED GENE | SCN1A |
| SYNONYMOUS | SCN1A |
| OMIM | 607208 |
| HEREDITY | Autosomal Dominant |
| CLINICAL AREA | Dravet Syndrome (DRVT) is an Autosomal Dominant inherited disease. Mutations in the SCN1A gene have been associated with the disease. |
| METHOD | Next Generation Sequencing |
| SAMPLE TYPE | Blood with EDTA |
| QUANTITY | 3 mL |
| TAT | 40 DAYS |
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