SPG-NGS

Paraplegias espásticas hereditárias - sequenciamento - 78 genes

Painel ampliado contendo 78 genes associados a paraplegias espásticas hereditárias

ABCD1, ADAR, AFG3L2, AIMP1, ALDH18A1, ALS2, AP4B1, AP4E1, AP4M1, AP4S1, AP5Z1, ARG1, ATL1, ATP13A2, B4GALNT1, BSCL2, C12orf65, C19orf12, CAPN1, CPT1C, CYP27A1, CYP2U1, CYP7B1, DARS, DDHD1, DDHD2, ENTPD1, ERLIN1, ERLIN2, FA2H, FARS2, FXN, GBA2, GCH1, HACE1, HIKESHI, HPDL, HSPD1, KCNA2, KDM5C, KIDINS220, KIF1A, KIF1C, KIF5A, L1CAM, MAG, NIPA1, NKX6-2, NT5C2, OPA3, PCYT2, PLP1, PNPLA6, POLR3A, PSEN1, REEP1, REEP2, RNASEH2B, RTN2, SACS, SELENOI, SERAC1, SLC16A2, SLC1A4, SLC25A46, SLC2A1, SPART, SPAST, SPG11, SPG21, SPG7, TFG, TUBB4A, UBAP1, UCHL1, WASHC5, WDR45B, ZFYVE26

40503801

40 a 60 dias úteis

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