MTM1 - X-linked myotubular myopathy type 1 (CNMX)

This test is available for the following conditions:

  • Conditions > Neuromuscular > Centronuclear myopathy

This product is also part of the following panels:

  • Fetal akinesia panel
  • Liver disorders panel
  • Mendelian inherited disorders panel
  • Metabolic disorders panel
  • Muscle 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: 300415
Performing laboratory: Radboudumc
Authorized material(s): EDTA blood, Isolated DNA, Buccal mucous membrane




€ 435

Gene

BIN1 - autosomal recessive centronuclear myopathy type 2

Turnaround time
Complete analysis: 8 weeks / Targeted analysis: 4 weeks
Performing laboratory
Radboudumc
€ 451

BIN1 - autosomal recessive centronuclear myopathy type 2



€ 451

BIN1 - autosomal recessive centronuclear myopathy type 2

This test is available for the following conditions:

  • Conditions > Neuromuscular > Centronuclear myopathy

This product is also part of the following panels:

  • Comprehensive preconception carrier test panel¹
  • Fetal akinesia panel
  • Mendelian inherited disorders panel
  • Muscle 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: 601248
Performing laboratory: Radboudumc
Authorized material(s): EDTA blood, Isolated DNA, Buccal mucous membrane




€ 451
Gene

DNM2 - centronuclear myopathie

Turnaround time
Complete analysis: 8 weeks / Targeted analysis: 4 weeks
Performing laboratory
Radboudumc
€ 492

DNM2 - centronuclear myopathie



€ 492

DNM2 - centronuclear myopathie

This test is available for the following conditions:

  • Conditions > Neuromuscular > Centronuclear myopathy

This product is also part of the following panels:

  • Comprehensive preconception carrier test panel¹
  • Fetal akinesia panel
  • Mendelian inherited disorders panel
  • Metabolic disorders panel
  • Mitochondrial disorders panel
  • Muscle disorders panel
  • Neuropathies panel¹

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

Method

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

OMIM: 602378
Performing laboratory: Radboudumc
Authorized material(s): EDTA blood, Isolated DNA, Buccal mucous membrane




€ 492
Gene

MTM1 - X-linked myotubular myopathy type 1 (CNMX)

Turnaround time
Complete analysis: 8 weeks / Targeted analysis: 4 weeks
Performing laboratory
Radboudumc
€ 435

MTM1 - X-linked myotubular myopathy type 1 (CNMX)



€ 435
Gene

MYF6 - centronuclear myopathie

Turnaround time
Complete analysis: 8 weeks / Targeted analysis: 4 weeks
Performing laboratory
Radboudumc
€ 336

MYF6 - centronuclear myopathie



€ 336

MYF6 - centronuclear myopathie

This test is available for the following conditions:

  • Conditions > Neuromuscular > Centronuclear myopathy

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

Method

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

OMIM: 159991
Performing laboratory: Radboudumc
Authorized material(s): EDTA blood, Isolated DNA, Buccal mucous membrane




€ 336