1. Genetic tests
  2. Alpha-1-antitrypsin deficiency (2 hot sopt mutations / p.Glu366Lys; p.Glu288Val )

Alpha-1-antitrypsin deficiency (2 hot sopt mutations / p.Glu366Lys; p.Glu288Val )

Genetic test Export to PDF
Full name:
Alpha-1-antitrypsin deficiency (2 hot sopt mutations / p.Glu366Lys; p.Glu288Val )
Test type:
Clinical
Test specialty:
Molecular Genetics
Test purpose:
Carrier diagnosis,
Post-natal Diagnosis
Specimen:
Peripheral (whole) blood on EDTA
Method category:
Targeted variant analysis
Method technique:
Real-time PCR
Laboratory:
Centrum Menselijke Erfelijkheid - KUL
RIZIV code:
565390-565401
Accreditation (ISO 15189):
2021-07-08 / 2026-02-02
Turnaround time (maximum):
6 - 10 weeks
Created:
17 Jul 2019 - 11:18
Changed:
01 Mar 2023 - 14:36
URL:
https://laboboeken.nexuzhealth.com/pboek/internet/GHB%20CME/12349