Rett Syndrome (Congenital)
| TEST CODE | MG02650 |
| TEST NAME | Rett Syndrome (Congenital) |
| RELATED GENE | FOXG1 |
| SYNONYMOUS | FOXG1 |
| OMIM | 613454 |
| HEREDITY | Autosomal Dominant |
| CLINICAL AREA | Rett Syndrome (Congenital) is a disease inherited as Autosomal Dominant. Mutations in the FOXG1 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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