NL
LRRK2 - Parkinson disease type 8
This test is available for the following conditions:
- Conditions > Neurological > Parkinson's disease
This product is also part of the following panels:
- Mendelian inherited disorders panel with genome wide CNV analysis
- 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:
609007
Performing laboratory: Radboudumc
Authorized material(s): EDTA blood, Isolated DNA, Buccal mucous membrane
PARK7 - autosomal recessive early-onset Parkinson disease type 7
This test is available for the following conditions:
- Conditions > Neurological > Parkinson's disease
This product is also part of the following panels:
- Comprehensive preconception carrier test panel¹
- Mendelian inherited disorders panel with genome wide CNV analysis
- 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:
602533
Performing laboratory: Radboudumc
Authorized material(s): EDTA blood, Isolated DNA, Buccal mucous membrane
PINK1 - autosomal recessive early-onset Parkinson disease type 6
This test is available for the following conditions:
- Conditions > Neurological > Parkinson's disease
This product is also part of the following panels:
- Comprehensive preconception carrier test panel¹
- Mendelian inherited disorders panel with genome wide CNV analysis
- 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:
608309
Performing laboratory: Radboudumc
Authorized material(s): EDTA blood, Isolated DNA, Buccal mucous membrane
