Deafness / hearing loss, autosomal dominant (extended panel)

ACTG1, CCDC50, CD164, CEACAM16, COCH, COL11A1, COL11A2, COL4A6, CRYM, DIABLO, DIAPH1, DIAPH3, DMXL2, EDN3, EDNRB, EYA4, FAM189A2, GJB2, GJB3, GJB6, GRHL2, GSDME, HOMER2, KCNQ4, KITLG, LMX1A, MCM2, MIR182, MIR183, MIR96, MITF, MYH14, MYH9, MYO6, MYO7A, NLRP3, OSBPL2, P2RX2, PAX3, PDE1C, PLS1, POU3F4, POU4F3, PRPS1, REST, SIX1, SLC17A8, SMPX, SOX10, TBC1D24, TECTA, TJP2, TMC1, TNC, WFS1

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