Hearing loss, nonsyndromal, autosomal recessive and X-linked.
Material: 1-2 ml of blood EDTA or 1-2 µg of genomic DNA
€1,400.00
Neurosensory nonsyndromal hearing loss, autosomal recessive and X-linked.
Non-syndromal forms account for the majority of inherited hearing loss (about 70%).
Set of genes included in the analysis: ADCY1, BDP1, BSND, CABP2, CDC14A, CDH23, CIB2, CLDN14, CLIC5, COL11A2, COL4A6, DCDC2, DFNB31, DFNB59, EPS8, EPS8L2, ESPN, ESRRB, FAM65B, G2 G2, G2 GJB3GJJJGGJGGJGGJGGJGGJGGJG3 GRXCR1, GRXCR2, HGF, ILDR1, KARS, LHFPL5, LOXHD1, LRTOMT, MARVELD2, MSRB3, MYO15A, MYO3A, MYO6, MYO7A, NARS2, OTOA, OTOF, OTOG, OTOGL, P0PTPPP3 P0PT3, MYT6A, OTOG, OTOG, PDO3 RDX, S1PR2, SERPINB6, SLC26A4, SLC26A5, SLITRK6, SMPX, STRC, SYNE4, TBC1D24, TECTA, TMC1, TMC2, TMEM132E, TMIE, TMPRSS3, TPRN, TRIOBP, TSPEAR, WP2, USHC
