1. Genetic tests
  2. Mitochondrial non-syndromic sensorineural deafness with susceptibility to aminoglycoside exposure (hot spot mutation - 1555A-G in MT-RNR1)

Mitochondrial non-syndromic sensorineural deafness with susceptibility to aminoglycoside exposure (hot spot mutation - 1555A-G in MT-RNR1)

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Full name:
Mitochondrial non-syndromic sensorineural deafness with susceptibility to aminoglycoside exposure (hot spot mutation - 1555A-G in MT-RNR1)
Test type:
Clinical
Test specialty:
Molecular Genetics
Test purpose:
Post-natal Diagnosis
Specimen:
Peripheral (whole) blood on EDTA
Method category:
Targeted variant analysis
Method technique:
Bi-directional Sanger Sequence analysis
Laboratory:
Centrum Medische Genetica - UZ Antwerpen
RIZIV code:
565390-565401
Accreditation (ISO 15189):
2023-11-09 / 2024-05-08
Turnaround time (maximum):
2 months
Document(s):
Created:
06 Aug 2019 - 13:11
Changed:
22 Jan 2024 - 14:01
URL:
https://labogidsmedgen.uza.be/analyses/slechthorendheid-mitochondriaal