Hereditäre Ataxien, umfassende Diagnostik : 128 Gene (373,050 kb)

ABCB7, ABHD12, ACO2, AFG3L2, AIFM1, ANGPTL1, ANO10, APOB, APTX, ATCAY, ATG5, ATG7, ATM, ATP1A3, ATP2B3, ATP8A2, CA8, CACNA1A, CACNA1G, CACNB4, CAPN1, CASK, CCDC88C, CHP1, CLCN2, CLN5, COA7, COQ2, COQ4, COQ8A, CWF19L1, CYP27A1, DAB1, DNMT1, EEF2, ELOVL4, ELOVL5, FAT2, FGF12, FGF14, FLVCR1, GDAP2, GOSR2, GRID2, GRM1, ITPR1, KCNA1, KCNC3, KCND3, KCNJ10, KIF1C, LAMA1, MARS2, MME, MRE11, MTCL1, MTPAP, MTTP, NBN, NKX6-2, NPTX1, OPHN1, PCDH12, PCNA, PDYN, PEX7, PHYH, PIK3R5, PITRM1, PLD3, PMPCA, PNKP, PNPLA6, POLG, POLR3A, POLR3B, PRDX3, PRKCG, PRPS1, PTF1A, PUM1, RFC1, RNF216, RNU12, RUBCN, SACS, SAMD9L, SCN2A, SCYL1, SETX, SIL1, SLC1A3, SLC2A1, SLC9A1, SLC9A6, SLC25A46, SLC52A2, SNX14, SPG7, SPTBN2, SQSTM1, STUB1, SYNE1, SYT14, TDP1, TDP2, TGM6, THG1L, TMEM240, TPP1, TRPC3, TSFM, TTBK2, TTPA, TUBB4A, TWNK, TXN2, UBA5, VAMP1, VLDLR, VPS13D, VPS41, VWA3B, WDR73, WDR81, WFS1, WWOX, XRCC1