Usher Syndrome Panel (10 Genes)
| TEST CODE | MGT0270 |
| TEST NAME | Usher Syndrome Panel (10 Genes) |
| RELATED GENE | ADGRV1, CDH23, CIB2, CLRN1, MYO7A, PCDH15, PDZD7, USH1C, USH1G, USH2A |
| SYNONYMOUS | ADGRV1, CDH23, CIB2, CLRN1, MYO7A, PCDH15, PDZD7, USH1C, USH1G, USH2A |
| OMIM | |
| HEREDITY | |
| CLINICAL AREA | Usher syndrome is an inherited disease characterized by progressive vision and hearing loss. While symptoms and disease progression vary from person to person, loss of balance is quite common. 10 genes associated with the disease are examined within the scope of the Usher Syndrome panel. |
| METHOD | Next Generation Sequencing (NGS) |
| SAMPLE TYPE | Blood with EDTA |
| QUANTITY | 3 mL |
| TAT | 40 DAYS |
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