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Deafness, autosomal recessive 1A

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Full name:
Deafness, autosomal recessive 1A
Test type:
Clinical
Test specialty:
Molecular Genetics
Test purpose:
Post-natal Diagnosis
Specimen:
Peripheral (whole) blood on EDTA
Method category:
Sequence analysis: entire coding region
Method technique:
Next Generation Sequencing (NGS)
Laboratory:
Centrum Medische Genetica - UZ Antwerpen
RIZIV code:
565456-565460
EQA:
  • 2017 Hereditary deafness EMQN
  • 2020 Hereditary deafness EMQN
  • 2023 Hereditary deafness EMQN
Accreditation (ISO 15189):
2023-11-09 / 2024-05-08
Turnaround time (maximum):
2 months
Document(s):
Created:
21 Aug 2019 - 09:06
Changed:
22 Jan 2024 - 13:43
URL:
https://labogidsmedgen.uza.be/analyses/slechthorendheid-prelinguaal-sensorineur…