RETT Syndrome
| TEST CODE | MG04530 |
| TEST NAME | RETT Syndrome |
| RELATED GENE | MECP2, CDKL5, ARX , NTNG1 |
| SYNONYMOUS | MECP2, CDKL5, ARX , NTNG1 |
| OMIM | 312750 |
| HEREDITY | X-linked Dominant |
| CLINICAL AREA | RETT Syndrome is an X-linked Dominant inherited disease. Mutations in the MECP2 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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