VCP - inclusion body myopathy with early-onset Paget disease and frontotemporal dementia

This test is available for the following conditions:

  • Conditions > Neuromuscular > Inclusion body myopathy

This product is also part of the following panels:

  • Amyotrophic lateral sclerosis, ALS panel
  • Intellectual disability panel with genome wide CNV analysis
  • Mendelian inherited disorders panel with genome wide CNV analysis
  • Movement disorders panel
  • Muscle disorders panel
  • Polyneuropathies panel¹

Turnaround time
Complete analysis: 8 weeks / Targeted analysis: 4 weeks

Method

  • Sequence analysis of all coding exons and flanking intron-exon boundaries

OMIM: 601023
Performing laboratory: Radboudumc
Authorized material(s): EDTA blood, Isolated DNA, Buccal mucous membrane




€ 426

Gene

VCP - inclusion body myopathy with early-onset Paget disease and frontotemporal dementia

Turnaround time
Complete analysis: 8 weeks / Targeted analysis: 4 weeks
Performing laboratory
Radboudumc
€ 426

VCP - inclusion body myopathy with early-onset Paget disease and frontotemporal dementia



€ 426