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  2. Hearing loss (deafness), autosomal dominant 9 (COCH exons 4 and 5)

Hearing loss (deafness), autosomal dominant 9 (COCH exons 4 and 5)

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Full name:
Hearing loss (deafness), autosomal dominant 9 (COCH exons 4 and 5)
Test type:
Clinical
Test specialty:
Molecular Genetics
Test purpose:
Post-natal Diagnosis
Specimen:
Peripheral (whole) blood on EDTA
Method category:
Mutation screening and sequence analysis of selected exons
Method technique:
Bi-directional Sanger Sequence analysis
Laboratory:
Centrum Medische Genetica - UZ Antwerpen
RIZIV code:
565456-565460
Accreditation (ISO 15189):
2023-11-09 / 2024-05-08
Turnaround time (maximum):
2 months
Document(s):
Created:
21 Aug 2019 - 09:03
Changed:
22 Jan 2024 - 13:56
URL:
https://labogidsmedgen.uza.be/analyses/slechthorendheid-niet-syndromaal-progres…