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TAT:

40

Tipo di Campione:

Metodica:

Analisi presente in:

Congenital Deafness – Panel

Geni/Polimorfismi:

ACTG1, ADGRV1/GPR98, AIFM1, ATP6V1B1, BSND, CCDC50, CDH23, CEACAM16, CIB2, CISD2, CLDN14, CLRN1, COCH, COL11A1, COL11A2, COL2A1, COL9A1, COL9A2, CRYM, DCDC2, DFNA5, DFNB31, DFNB59, DIABLO, DIAPH1, DIAPH3, EDN3, EDNRB, ESPN, ESRRB, EYA1, EYA4, FOXI1, GIPC3, GJB2/CX26, GJB3, GJB6/CX30, GRHL2, GRXCR1, HARS, HGF, HOMER2, ILDR1, KARS, KCNE1, KCNJ10, KCNQ1, KCNQ4, KITLG, LHFPL5, LOXHD1, LRTOMT, MARVELD2, MET, MIR96, MITF, MSRB3, MYH14, MYH9, MYO15A, MYO3A, MYO6, MYO7A, NARS2, OPA1, OTOA, OTOF, PAX3, PCDH15, PDZD7, POLR1C, POLR1D, POU3F4, POU4F3, PRPS1, PTPRQ, RDX, SERPINB6, SIX1, SIX5, SLC17A8, SLC26A4, SLC26A5, SMPX, SNAI2, SOX10, STRC, TBC1D24, TCOF1, TECTA, TJP2, TMC1, TMIE, TMPRSS3, TNC, TPRN, TRIOBP, USH1C, USH1G, USH2A, WFS1

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