Molybdenum Cofactor Deficiency Type C
| TEST CODE | MG08660 |
| TEST NAME | Molybdenum Cofactor Deficiency Type C |
| RELATED GENE | GPHN |
| SYNONYMOUS | GPHN |
| OMIM | 603930 |
| HEREDITY | Autosomal Recessive |
| CLINICAL AREA | Molybdenum Cofactor Deficiency Type C is an Autosomal Recessively inherited disease. Mutations in the GPHN 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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