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VEXAS-syndrome

Genetic test Export to PDF
Full name:
VEXAS-syndrome
Description:

UBA1 p.(Met41))
Test type:
Clinical
Test specialty:
Molecular Genetics
Test purpose:
Mutation confirmation,
Post-natal Diagnosis
Specimen:
Peripheral (whole) blood on EDTA,
Bone marrow
Method category:
Targeted variant analysis
Method technique:
Next Generation Sequencing (NGS)
Laboratory:
Centrum Medische Genetica - UZ Gent
RIZIV code:
565390-565401
Turnaround time (maximum):
4-6 weeks
Created:
12 Dec 2022 - 14:44
Changed:
10 Jan 2024 - 14:27