Hearing loss, nonsyndromal, autosomal dominant 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: ACTG1, CCDC50, CD164, CEACAM16, COCH, COL11A2, COL4A6, CRYM, DFNA5, DIABLO, DIAPH1, DIAPH3, ESPN, EYA4, GJB2, GJB3, GJB6, GRHL2, MY6, MY6, MJ9, M6, M96, K9 OSBPL2, P2RX2, POU3F4, POU4F3, PRPS1, SLC17A8, SMPX, TBC1D24, TECTA, TJP2, TMC1, TMC2, TNC, WFS1
