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Friedreich ataxia - GAA repeat expansion

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Full name:
Friedreich ataxia - GAA repeat expansion
Test type:
Clinical
Test specialty:
Molecular Genetics
Test purpose:
Carrier diagnosis,
Post-natal Diagnosis,
Predictive and Pre-symptomatic diagnosis,
Prenatal diagnosis
Specimen:
Peripheral (whole) blood on EDTA,
Amniotic fluid,
Chorionic villi
Method category:
Targeted variant analysis
Method technique:
PCR based technique
Laboratory:
Centrum Menselijke Erfelijkheid - KUL
RIZIV code:
565456-565460
EQA:
  • 2017 Friedreich Ataxia EMQN
  • 2020 Friedreich Ataxia EMQN
Accreditation (ISO 15189):
2021-07-08 / 2026-02-02
Turnaround time (maximum):
6 - 13 weeks
Document(s):
Created:
19 Jul 2019 - 11:16
Changed:
01 Mar 2023 - 15:01
URL:
https://laboboeken.nexuzhealth.com/pboek/internet/GHB%20CME/15311