Central Hypoventilation Syndrome
| TEST CODE | MG00730 |
| TEST NAME | Central Hypoventilation Syndrome |
| RELATED GENE | ASCL1 |
| SYNONYMOUS | ASCL1 |
| OMIM | 100790 |
| HEREDITY | Autosomal Dominant |
| CLINICAL AREA | Central Hypoventilation Syndrome is an Autosomal Dominant inherited disease. Mutations in the ASCL1 gene have been associated with the disease. |
| METHOD | Next Generation Sequencing |
| SAMPLE TYPE | Blood with EDTA |
| QUANTITY | 3 mL |
| TAT | 21 DAYS |
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