Genes | ALS2, ANG, APOE, APP, ATP7B, C19orf12, CHCHD10, CHMP2B, CLN3, CLN5, CP, CSF1R, CTSD, CTSF, EIF4G1, ERBB4, FUS, GIGYF2, GRN, HNRNPA1, HNRNPA2B1, HTRA1, ITM2B, MAPT, NOTCH3, NPC1, NPC2, OPTN, PDGFB, PDGFRB, PPT1, PRKAR1B, PRNP, PSEN1, PSEN2, PSENEN, SERPINI1, SETX, SIGMAR1, SLC20A2, SNCA, SNCB, SOD1, SORL1, SPG11, SQSTM1, TARDBP, TBK1, TREM2, TYROBP, UBQLN2, VCP, VPS13A, XPR1 |
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Lab method | Del/Dup Analysis, NGS Sequencing |
Turnaround time | 3 months |
Location | Location VU |
Price | € 1.440,00 |
AGDx NGS – Dementia ALS panel v4 plus CNV
Test code: V00254Disorder(s)
- Alzheimer Disease
- Amyotrophic lateral sclerosis 10 - with or without FTD (OMIM: 612069)
- Dementia - Lewy body (OMIM: 127750)
- Frontotemporal Dementia - FTD (OMIM: 600274)
- Frontotemporal dementia and/or amyotrophic lateral sclerosis 1 - FTDALS1 (OMIM: 105550)
- Frontotemporal lobar degeneration with ubiquitin-positive inclusions (OMIM: 607485)
- Pick disease (OMIM: 172700)