UQCRB - Mitochondrial complex III deficiency

This test is available for the following conditions:

  • Conditions > Mitochondrial disorders > Complex III deficiency

This product is also part of the following panels:

  • Comprehensive preconception carrier test panel¹
  • Comprehensive preconception carrier test panel¹
  • Mendelian inherited disorders panel with genome wide CNV analysis
  • Mendelian inherited disorders panel with genome wide CNV analysis
  • Mitochondrial disorders panel
  • Mitochondrial 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: 191330
Performing laboratory: Radboudumc
Authorized material(s): EDTA blood, Isolated DNA, Buccal mucous membrane




€ 725

Gene

BCS1 - Mitochondrial complex III deficiency

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

BCS1 - Mitochondrial complex III deficiency



€ 725

BCS1 - Mitochondrial complex III deficiency

This test is available for the following conditions:

  • Conditions > Mitochondrial disorders > Complex III deficiency

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

Method

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

OMIM: 603647
Performing laboratory: Radboudumc
Authorized material(s): EDTA blood, Isolated DNA, Buccal mucous membrane




€ 725
Gene

CYC1 - Mitochondrial complex III deficieny

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

CYC1 - Mitochondrial complex III deficieny



€ 725

CYC1 - Mitochondrial complex III deficieny

This test is available for the following conditions:

  • Conditions > Mitochondrial disorders > Complex III deficiency

This product is also part of the following panels:

  • Comprehensive preconception carrier test panel¹
  • Comprehensive preconception carrier test panel¹
  • Mendelian inherited disorders panel with genome wide CNV analysis
  • Mendelian inherited disorders panel with genome wide CNV analysis
  • Mitochondrial disorders panel
  • Mitochondrial 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: 123980
Performing laboratory: Radboudumc
Authorized material(s): EDTA blood, Isolated DNA, Buccal mucous membrane




€ 725
Gene

UQCC3 - Mitochondrial complex III deficiency

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

UQCC3 - Mitochondrial complex III deficiency



€ 725

UQCC3 - Mitochondrial complex III deficiency

This test is available for the following conditions:

  • Conditions > Mitochondrial disorders > Complex III deficiency

This product is also part of the following panels:

  • Comprehensive preconception carrier test panel¹
  • Comprehensive preconception carrier test panel¹
  • Mendelian inherited disorders panel with genome wide CNV analysis
  • Mendelian inherited disorders panel with genome wide CNV analysis
  • Mitochondrial disorders panel
  • Mitochondrial 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: 616097
Performing laboratory: Radboudumc
Authorized material(s): EDTA blood, Isolated DNA, Buccal mucous membrane




€ 725
Gene

UQCRB - Mitochondrial complex III deficiency

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

UQCRB - Mitochondrial complex III deficiency



€ 725