panel erythrokeratodermia variabilis (GJB3, GJB4)¹
This test is available for the following conditions:
- Conditions > Skin > Erythrokeratodermia variabilis
Turnaround time
8 weeks
Method
- Sequence analysis of all coding exons and flanking intron-exon boundaries
Performing laboratory: Maastricht UMC+
Authorized material(s): EDTA blood, Isolated DNA
GJB3 - erythrokeratodermia variabilis ¹
This test is available for the following conditions:
- Conditions > Skin > Erythrokeratodermia variabilis
This product is also part of the following panels:
- Comprehensive preconception carrier test panel¹
- Hearing impairment panel (including GJB2)
- Mendelian inherited disorders panel with genome wide CNV analysis
- Neuropathies panel¹
- panel erythrokeratodermia variabilis (GJB3, GJB4)¹
- 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:
603324
Performing laboratory: Maastricht UMC+
Authorized material(s): EDTA blood, Isolated DNA, Buccal mucous membrane