Liddle Syndrome
| TEST CODE | MG01740 |
| TEST NAME | Liddle Syndrome |
| RELATED GENE | SCNN1B |
| SYNONYMOUS | SCNN1B |
| OMIM | 177200 |
| HEREDITY | Autosomal Dominant |
| CLINICAL AREA | Liddle Syndrome (LIDLS1) is an autosomal dominantly inherited disease. Mutations in the SCNN1B 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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