HADHB - Mitochondrial trifunctional protein deficiency 2

This test is available for the following conditions:

  • Conditions > Metabolic disorders > Mitochondrial trifunctional protein deficiency 2

This product is also part of the following panels:

  • Comprehensive preconception carrier test panel¹
  • Heart disorders panel¹
  • Intellectual disability panel with genome wide CNV analysis
  • Mendelian inherited disorders panel with genome wide CNV analysis
  • Metabolic disorders panel
  • Mitochondrial disorders panel
  • Muscle disorders panel
  • Polyneuropathies panel¹

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

Method

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

OMIM: 143450
Performing laboratory: Radboudumc
Authorized material(s): EDTA blood, Isolated DNA, Buccal mucous membrane



€ 725
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Gene

HADHB - Mitochondrial trifunctional protein deficiency 2

Turnaround time
Complete analysis: 8 weeks / Targeted analysis: 4 weeks
Performing laboratory
Radboudumc
€ 725
View Add

HADHB - Mitochondrial trifunctional protein deficiency 2


€ 725
Add