OXCT1 - Succinyl CoA3-oxoacid CoA transferase deficiency
This test is available for the following conditions:
- Conditions > Metabolic disorders > Succinyl CoA3-oxoacid CoA transferase deficiency
 
This product is also part of the following panels:
- Comprehensive preconception carrier test panel¹
 - Mendelian inherited disorders panel with genome wide CNV analysis
 - Metabolic 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: 
601424                    
                    Performing laboratory: Radboudumc
                    Authorized material(s): EDTA blood, Isolated DNA, Buccal mucous membrane