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Deafness, autosomal dominant 6/14 / Wolfram syndrome

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Full name:
Deafness, autosomal dominant 6/14 / Wolfram syndrome
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:
565471-565482
Accreditation (ISO 15189):
2023-11-09 / 2024-05-08
Turnaround time (maximum):
Unknown
Document(s):
Created:
21 Aug 2019 - 08:57
Changed:
22 Jan 2024 - 13:42