Autosomal dominant non-syndromic hearing loss, NGS
Detect autosomal dominant genetic causes of non-syndromic hearing loss; familial risk management.
Genelist (46): ACTG1, CCDC50, CD164, CEACAM16, COCH, COL11A2, CRYL1, CRYM, DIABLO, DIAPH1, DIAPH3, DSPP, ELMOD3, EYA1, EYA4, GJB2, GJB3, GJB6, GRHL2, GSDME, HOMER2, KCNQ4, KITLG, MIR96, MYH14, MYH9, MYO6, MYO7A, OSBPL2, P2RX2, PNPT1, POU4F3, PRPS1, PTPRR, RIPOR2, SIX1, SLC17A8, SMPX, TBC1D24, TECTA, TJP2, TMC1, TMC2, TNC, WFS1, WHRN
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Detect autosomal dominant genetic causes of non-syndromic hearing loss; familial risk management.
Genelist (46): ACTG1, CCDC50, CD164, CEACAM16, COCH, COL11A2, CRYL1, CRYM, DIABLO, DIAPH1, DIAPH3, DSPP, ELMOD3, EYA1, EYA4, GJB2, GJB3, GJB6, GRHL2, GSDME, HOMER2, KCNQ4, KITLG, MIR96, MYH14, MYH9, MYO6, MYO7A, OSBPL2, P2RX2, PNPT1, POU4F3, PRPS1, PTPRR, RIPOR2, SIX1, SLC17A8, SMPX, TBC1D24, TECTA, TJP2, TMC1, TMC2, TNC, WFS1, WHRN