KCNJ2 - Andersen syndrome¹

This test is available for the following conditions:

  • Conditions > Cardiovascular > Anderson syndrome

This product is also part of the following panels:

  • Arrhythmia and cardiac conduction disorders panel¹
  • Heart disorders panel¹
  • Long QT syndrome panel¹
  • Mendelian inherited disorders panel with genome wide CNV analysis
  • Muscle disorders panel
  • Orofacial clefting panel with genome wide CNV analysis
  • Short stature/skeletal dysplasia panel with genome wide CNV analysis

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

Method

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

OMIM: 600681
Performing laboratory: Maastricht UMC+
Authorized material(s): EDTA blood, Isolated DNA, Buccal mucous membrane



€ 380
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Gene

KCNJ2 - Andersen syndrome¹

Turnaround time
Complete analysis: 8 weeks / Targeted analysis: 4 weeks
Performing laboratory
Maastricht UMC+
€ 380
View Add

KCNJ2 - Andersen syndrome¹


€ 380
Add