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Table 2 HSP and CMT genes checked

From: SPG9A with the new occurrence of an ALDH18A1 mutation in a CMT1A family with PMP22 duplication: case report

(ATL1, SPAST, NIPA1, KIAA0196, ALDH18A1, KIF5A, RTN2, HSPD1, BSCL2, ATSV, REEP1, ZFYVE27, SLC33A1, REEP2, CPT1C, CYP7B1, SPG7, SPG11, ZFYVE26, ERLIN2, SPG20, ACP33, B4GALNT1, DDHD1, FA2H, PNPLA6, c9orf12, GJA2, AP4B1, KIAA0415, TECPR2, AP4M1, AP4E1, AP4S1, VPS37A, DDHD2, c12orf65, CYP2U1, TFG, KIF1C, USP8, WDR48, ARL6IP1, ERLIN1, AMPD2, ENTPD1, ARSI, PGAP1, FLRT1, RAB3GAP2, MARS, ZFR, IBA57, MAG, MPZ, LITAF, EGR2, NEFL, FBLN5, KARS, SOX10, GJB3, ARHGEF10,G GNB4, HARS, GDAP, MTMR2, SBF2, SBF1, SH3TC2, NDRG1, EGR2, PRX, HK1, FGD4, FIG 4, SURF1, CTDP1, ASAH1, PMM2, GALC, ARSA, PHYH, PEX7, ABHD12, DNAJC3, GJB1, MFN2, KIF1B, RAB7, TRPV4, GARS, HSPB1, GDAP1, HSPB8, DNM2, AARS, DYNC1H1, LRSAM1, DHT, DNAJB2, MARS, NAGLU, HARS, VCP, MORC2, LMNA, MED25, HSPB1, DNM2, YARS, INF2, GNB4, GDAP)