Gorlin-Goltz Syndrome
| TEST CODE | MG01210 |
| TEST NAME | Gorlin-Goltz Syndrome |
| RELATED GENE | PTCH1 |
| SYNONYMOUS | PTCH1 |
| OMIM | 109400 |
| HEREDITY | Autosomal Dominant |
| CLINICAL AREA | Gorlin-Goltz Syndrome is an autosomal dominantly inherited disease. Mutations in the PTCH1 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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