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Mc Ardle disease, glycogene storage disease type V

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Full name:
Mc Ardle disease, glycogene storage disease type V
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:
Bi-directional Sanger Sequence analysis
Laboratory:
Centre de Génétique Humaine - CHU Sart-Tilman
RIZIV code:
565471-565482
Turnaround time (maximum):
1 month
Document(s):
Created:
02 Sep 2019 - 07:49
Changed:
02 Jan 2023 - 17:00
URL:
https://www.chu.ulg.ac.be/jcms/c2_23256207/fr/glycogenose-par-deficit-en-glycog…