LMNA - Lamin A/C nucleair staining ¹

This test is available for the following conditions:

  • Conditions > Cardiovascular > Laminopathy
  • Conditions > Cardiovascular > Limb-Girdle, Emery Dreifuss

Turnaround time
4 months

Method

  • Functional test

OMIM: 150330
Performing laboratory: Maastricht UMC+
Authorized material(s): Skin biopsy, Fibroblast




€ 410

Gene

LMNA - Lamin A/C nucleair staining ¹

Turnaround time
4 months
Performing laboratory
Maastricht UMC+
€ 410

LMNA - Lamin A/C nucleair staining ¹



€ 410
Gene

LMNA - Laminopathy ¹

Turnaround time
Complete analysis: 8 weeks / Targeted analysis: 4 weeks
Performing laboratory
Maastricht UMC+
€ 410

LMNA - Laminopathy ¹



€ 410

LMNA - Laminopathy ¹

This test is available for the following conditions:

  • Conditions > Cardiovascular > Laminopathy

This product is also part of the following panels:

  • Arrhythmia and cardiac conduction disorders panel¹
  • Comprehensive preconception carrier test panel¹
  • Dilated cardiomyopathy panel¹
  • Fetal akinesia panel
  • Heart disorders panel¹
  • Mendelian inherited disorders panel with genome wide CNV analysis
  • Metabolic disorders panel
  • Muscle disorders panel
  • Neuropathies panel¹
  • Short stature/skeletal dysplasia panel with genome wide CNV analysis
  • Skin disorders panel¹

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

Method

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

OMIM: 150330
Performing laboratory: Maastricht UMC+
Authorized material(s): EDTA blood, Isolated DNA, Buccal mucous membrane




€ 410
Gene

ZMPSTE24 - Laminopathy ¹

Turnaround time
Complete analysis: 8 weeks / Targeted analysis: 4 weeks
Performing laboratory
Maastricht UMC+
€ 393

ZMPSTE24 - Laminopathy ¹



€ 393

ZMPSTE24 - Laminopathy ¹

This test is available for the following conditions:

  • Conditions > Cardiovascular > Laminopathy

This product is also part of the following panels:

  • Comprehensive preconception carrier test panel¹
  • Fetal akinesia panel
  • Mendelian inherited disorders panel with genome wide CNV analysis
  • Metabolic disorders panel
  • Orofacial clefting panel with genome wide CNV analysis
  • Renal disorders panel
  • Short stature/skeletal dysplasia panel with genome wide CNV analysis
  • Skin disorders panel¹

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

Method

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

OMIM: 606480
Performing laboratory: Maastricht UMC+
Authorized material(s): EDTA blood, Isolated DNA, Buccal mucous membrane




€ 393