Alpha Thalassemia Deletion Test-HBA(*)
| TEST CODE | MG00030 |
| TEST NAME | Alpha Thalassemia Deletion Test-HBA(*) |
| RELATED GENE | HBA |
| SYNONYMOUS | HBA |
| OMIM | 604131 |
| HEREDITY | Autosomal Dominant/Autosomal Recessive |
| CLINICAL AREA | Alpha thalassemia is a disease that is inherited in an autosomal recessive and dominant manner. Mutations in the HBA gene have been associated with the disease. This test screens for deletion/duplication type mutations in the disease-related gene using the MLPA method. |
| METHOD | MLPA |
| SAMPLE TYPE | Blood with EDTA |
| QUANTITY | 3 ml |
| TAT | 40 DAYS |
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