Mitochondrial Deletion Panel (Kearn Sayre Syndrome)
| TEST CODE | MG01890 |
| TEST NAME | Mitochondrial Deletion Panel (Kearn Sayre Syndrome) |
| RELATED GENE | MT – DNA |
| SYNONYMOUS | MT – DNA |
| OMIM | |
| HEREDITY | Mitochondrial Inheritance |
| CLINICAL AREA | Kearn Sayre Syndrome is a mitochondrially inherited disease. Mutations in the MT-TL1 and mitochondrial tRNA genes 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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