Panel

ADAR Analysis AIFM1 selected exon sequencing AIMP1 Analysis ANG Analysis APP Analysis AUTS2 Analysis BSCL2 Analysis C9ORF72 Repeat analysis CASK Analysis CHMP2B Analysis CLCN2 Analysis CSF1R Analysis CTC1 Analysis CTDP1 Analysis CTSF Analysis DJ-1 (PARK7) Analysis DNM2 Analysis EGR2 Analysis EXOSC3 Analysis FA2H Analysis FAM126A Analysis FGD4 Analysis FIG4 Analysis FMR1-CGG Repeat analysis FUS Analysis GARS1 Analysis GDAP1 Analysis GJB1 Analysis GJC2 Analysis GRN (PGRN) Analysis HDAC8 Analysis HEPACAM Analysis HSPB1 Analysis HSPB8 Analysis HSPB8 Analysis (HMN) HSPD1 Analysis IFIH1 Analysis IGHMBP2 Analysis LITAF Analysis LMNA Analysis LMNB1 MLPA LRRK2 (PARK8) Analysis LRSAM1 Analysis MAPT Analysis Methylering Chr.15q11 MFN2 Analysis Microdeleties MLPA MPZ Analysis MTM1 Analysis MTMR2 Analysis NDRG1 Analysis NEFL Analysis NGF Analysis NGS Amyotrofe Lateraal Sclerose ALS NGS Bewegingsstoornissen NGS Cornelia de Lange NGS Dementie NGS Dementie risicofactoren NGS Epilepsie NGS Intellectual disability NGS Neurodegeneration with brain iron accumulation NBIA NGS Neuropathy/Charcot Marie Tooth NGS Parkinson NGS Pontocerebellaire hypoplasie PCH NGS Wittestofziekten NIPBL Analysis NKX2-1 Analysis PARKIN (PARK2) Analysis PCH Volendamse founder mutatie PINK1 (PARK6) Analysis PLP1 Analysis PLP1 Del/Dup analysis PMP22 Analysis PMP22 Del/Dup analysis POLR1C Analysis POLR3A Analysis POLR3B Analysis PRNP Analysis PSEN1 Analysis PSEN2 Analysis RAB7A Analysis RARS2 Analysis RNASEH2A Analysis RNASEH2B Analysis RNASEH2C Analysis RNASET2 Analysis SAMHD1 Analysis SEPTIN9 Analysis SETX Analysis SGCE Analysis SH3TC2 Analysis SHANK3 Analysis SMC1A Analysis SNCA (PARK1) Analysis SNORD118 Analysis SOD1 Analysis SPTLC1 Analysis TARDBP Analysis THAP1 Analysis TMEM106B Analysis TMEM63A Analysis TOE1 Analysis TOR1A Analysis TREX1 Analysis TRPV4 Analysis TSEN2 Analysis TSEN34 Analysis TSEN54 Analysis TUBB4A Analysis UFM1 Select exon sequencing UPD Chr.15 VCP Analysis VRK1 Analysis WBS MLPA WNK1 Analysis