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WFS1

Exames relacionados Estratégia de Análise Gene relacionado
Wolfram, Síndrome Painel por Sequenciamento de Próxima Geração CISD2, WFS1
Surdez Não Sindrômica, Autossômica Dominante Painel por Sequenciamento de Próxima Geração ACTG1, CCDC50, COCH, COL11A2, DFNA5, DIAPH1, EYA4, GJB2, GJB3, GJB6, GRHL2, KCNQ4, MYH14, MYH9, MYO1A, MYO6, MYO7A, POU4F3, SLC17A8, TECTA, TMC1, WFS1
Retinite Pigmentosa Painel por Sequenciamento de Próxima Geração ABCA4, AIPL1, ARL6, BBS1, BBS10, BBS12, BBS2, BBS4, BBS5, BBS7, BBS9, BEST1, C2ORF71, C8ORF37, CA4, CACNA1F, CDH23, CEP290, CERKL, CLRN1, CNGA1, CNGB1, CRB1, CRX, DFNB31, DHDDS, EYS, FAM161A, FLVCR1, FSCN2, GNPTG, GUCA1B, GUCY2D, IDH3B, IMPDH1, IMPG2, INVS, IQCB1, KLHL7, LRAT, MAK, MERTK, MKKS, NPHP1, NPHP3, NPHP4, NR2E3, NRL, PCDH15, PDE6A, PDE6B, PDE6G, PEX1, PEX2, PEX26, PEX7, PHYH, PRCD, PROM1, PRPF3, PRPF31, PRPF6, PRPF8, PRPH2, RBP3, RDH12, RGR, RHO, RLBP1, ROM1, RP1, RP2, RP9, RPE65, RPGR, RPGRIP1L, SAG, SEMA4A, SNRNP200, SPATA7, TOPORS, TRIM32, TTC8, TULP1, USH1C, USH2A, WFS1, ZNF513
Epilepsia Painel por Sequenciamento de Próxima Geração SLC6A8, SLC9A6, SMC1A, SPR, SPTAN1, ST3GAL3, ST3GAL5, STXBP1, SUOX, SYN1, TBC1D24, TCF4, TPP1, TSC1, TSC2, UBE3A, UBR5, WFS1, ZEB2
Epilepsia, Painel Expandido Painel por Sequenciamento de Próxima Geração CACNA1A, CASR, GABRD, ASAH1, KCNMA1, ME2, PRICKLE2, SLC4A10, SMC1A, SPR, ST3GAL3, ST3GAL5, SUOX, UBR5, WFS1, ADSL, ALDH7A1, ALG13, ARHGEF9, ARX, ATP1A2, CACNA2D2, CDKL5, CHD2, CHRNA2, CHRNA4, CHRNB2, CLN3, CLN5, CLN6, CLN8, CNTNAP2, CSTB, CTSD, DEPDC5, DNAJC5, DYNC1H1, EFHC1, EPM2A, FOLR1, FOXG1, GABRA1, GABRB3, GABRG2, GAMT, GATM, GNAO1, GOSR2, GRIN1, GRIN2A, GRIN2B, HCN1, HNRNPU, KANSL1, KCNH2, KCNJ10, KCNQ2, KCNQ3, KCNT1, KCTD7, LGI1, LIAS, MBD5, MECP2, MEF2C, MFSD8, NHLRC1, NRXN1, PCDH19, PLCB1, PNKP, PNPO, POLG, PPT1, PRICKLE1, PRRT2, QARS, RBFOX1, ROGDI, SCARB2, SCN1A, SCN1B, SCN2A, SCN3A, SCN5A, SCN8A, SCN9A, SLC25A22, SLC2A1, SLC35A2, SLC6A8, SLC9A6, SPTAN1, STXBP1, SYN1, SYNGAP1, TBC1D24, TCF4, TPP1, TSC1, TSC2, UBE3A, ZEB2, WWOX, NPR2L, STX1B, CNTN2, CACNB4, CACNA1H, CLCN2, ADRA2B, SNIP1, CPA6, IER3IP1, STRADA, SLC6A1, LNPK, ICK, TRAPPC6B, NACC1, PROSC, NPRL3, PRDM8, SLC12A5, LMNB2, SPATA5, RELN, GAL, CERS1, KCNC1, SRPX2, CRH, NPRL2
Atrofia Óptica, Painel Expandido Painel por Sequenciamento de Próxima Geração ACO2, AUH, C12ORF65, CISD2, MFN2, MTPAP, NDUFS1, NR2F1, OPA1, OPA3, POLG, SLC24A1, SPG7, TIMM8A, TMEM126A, WFS1
Subscrever WFS1