PRRT2 - familial infantile convulsions with paroxysmal choreoathetosis

This test is available for the following conditions:

  • Conditions > Neurological > Familial infantile convulsions with paroxysmal choreoathetosis

This product is also part of the following panels:

  • Epilepsy panel
  • Mendelian inherited disorders panel with genome wide CNV analysis
  • Movement disorders panel

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

Method

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

OMIM: 602066
Performing laboratory: Radboudumc
Authorized material(s): EDTA blood, Isolated DNA, Buccal mucous membrane




€ 353

Gene

PRRT2 - familial infantile convulsions with paroxysmal choreoathetosis

Turnaround time
Complete analysis: 8 weeks / Targeted analysis: 4 weeks
Performing laboratory
Radboudumc
€ 353

PRRT2 - familial infantile convulsions with paroxysmal choreoathetosis



€ 353