Autosomal Recessive Nonsyndromic Hearing Loss Panel (42 Genes)
| TEST CODE | MGT0040 |
| TEST NAME | Autosomal Recessive Nonsyndromic Hearing Loss Panel (42 Genes) |
| RELATED GENE | CDH23, CLDN14, COL11A2, DFNB31, DFNB59, ESPN, ESRRB, FOXI1, GIPC3, GJB2, GJB3, GJB6, GPSM2, GRXCR1, HGF, ILDR1, KCNJ10, LHFPL5, LOXHD1, LRTOMT, MARBELD2, MSRB3, MYO15A, MYO3A, MYO6, MYO7A, OTA, OTOF, PCDH15, PTPRQ, RDX, SERPINB6, SLC12A1, SLC26A4, STRC, TECTA, TMC1, TMIE, TMPRSS3, TPRN, TRIOBP, USH1C |
| SYNONYMOUS | CDH23, CLDN14, COL11A2, DFNB31, DFNB59, ESPN, ESRRB, FOXI1, GIPC3, GJB2, GJB3, GJB6, GPSM2, GRXCR1, HGF, ILDR1, KCNJ10, LHFPL5, LOXHD1, LRTOMT, MARBELD2, MSRB3, MYO15A, MYO3A, MYO6, MYO7A, OTA, OTOF, PCDH15, PTPRQ, RDX, SERPINB6, SLC12A1, SLC26A4, STRC, TECTA, TMC1, TMIE, TMPRSS3, TPRN, TRIOBP, USH1C |
| OMIM | |
| HEREDITY | |
| CLINICAL AREA | Nonsyndromic hearing loss is partial or complete hearing loss that is not associated with any signs or symptoms. It accounts for 70% of genetic hearing losses. 42 disease-related genes inherited as Autosomal Recessive are examined within the scope of the panel. |
| METHOD | Next Generation Sequencing (NGS) |
| SAMPLE TYPE | Blood with EDTA |
| QUANTITY | 3 mL |
| TAT | 40 DAYS |
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