C19ORF12 - Spastic paraplegia- autosomal recessive
This test is available for the following conditions:
- Conditions > Mitochondrial disorders > Spastic paraplegia, autosomal recessive
- Conditions > Neurological > Spastic paraplegia, autosomal recessive
Turnaround time
Complete analysis: 8 weeks / Targeted analysis: 4 weeks
Method
- Sequence analysis of all coding exons and flanking intron-exon boundaries
OMIM:
614297
Performing laboratory: Radboudumc
Authorized material(s): EDTA blood, Isolated DNA, Buccal mucous membrane