ATP1A3 - CAPOS syndrome

This test is available for the following conditions:

  • Conditions > Neurological > CAPOS syndrome
  • Conditions > Vision impairment / blindness > CAPOS syndrome

This product is also part of the following panels:

  • Epilepsy panel
  • Hearing impairment panel (including GJB2)
  • Intellectual disability panel with genome wide CNV analysis
  • Mendelian inherited disorders panel with genome wide CNV analysis
  • Movement disorders panel
  • Parkinson disease panel

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

Method

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

OMIM: 601338
Performing laboratory: Radboudumc
Authorized material(s): EDTA blood, Isolated DNA, Buccal mucous membrane




€ 460

Gene

ATP1A3 - CAPOS syndrome

Turnaround time
Complete analysis: 8 weeks / Targeted analysis: 4 weeks
Performing laboratory
Radboudumc
€ 460

ATP1A3 - CAPOS syndrome



€ 460