Liddle Sendromu
| TEST CODE | MG01730 |
| TEST NAME | Liddle Sendromu |
| RELATED GENE | SCNN1G |
| SYNONYMOUS | SCNN1G |
| OMIM | 618114 |
| HEREDITY | Autosomal Dominant |
| CLINICAL AREA | Liddle Syndrome (LIDLS2) is a disease inherited in an autosomal dominant manner. Mutations in the SCNN1G gene have been associated with the disease. |
| METHOD | Next Generation Sequencing |
| SAMPLE TYPE | Blood with EDTA |
| QUANTITY | 3 mL |
| TAT | 40 DAYS |
ORDER OPTIONS AND PRICING
Discover genetic insights at your convenience. Contact Mikrogen anytime for information on order options, pricing, and comprehensive genetic testing services