Lipoprotein A (LPA Exon 1-39) Panel
| TEST CODE | MG04630 |
| TEST NAME | Lipoprotein A (LPA Exon 1-39) Panel |
| RELATED GENE | LPA |
| SYNONYMOUS | LPA |
| OMIM | 618807 |
| HEREDITY | Autosomal Dominant |
| CLINICAL AREA | Congenital Lipoprotein A Deficiency is an autosomal dominantly inherited disease. Mutations in the LPA gene have been associated with the disease. |
| METHOD | Next Generation Sequencing |
| SAMPLE TYPE | Blood with EDTA |
| QUANTITY | 3 ml |
| TAT | 40 DAYS |
ORDER OPTIONS AND PRICING
Discover genetic insights at your convenience. Contact Mikrogen anytime for information on order options, pricing, and comprehensive genetic testing services