PRRT2 - benign familial infantile seizures type 2
This test is available for the following conditions:
- Conditions > Neurological > Benign familial infantile seizures
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:
605751
Performing laboratory: Radboudumc
Authorized material(s): EDTA blood, Isolated DNA, Buccal mucous membrane