SCN1A MLPA
| TEST CODE | MG09270 |
| TEST NAME | SCN1A MLPA |
| RELATED GENE | SCN1A |
| SYNONYMOUS | SCN1A |
| OMIM | 182389 |
| HEREDITY | Autosomal Dominant |
| CLINICAL AREA | SCN1A is an autosomal dominantly inherited disease. Mutations in the SCN1A gene have been associated with the disease. This test screens for deletion/duplication type mutations in the disease-related gene using the MLPA method. |
| METHOD | MLPA |
| SAMPLE TYPE | Blood with EDTA |
| QUANTITY | 3 ml |
| TAT | 40 DAYS |
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