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Amyloidosis hereditary / Dystransthyretinemic hyperthyroxinemia

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Full name:
Amyloidosis hereditary / Dystransthyretinemic hyperthyroxinemia
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
Deletion/duplication analysis
Method technique:
Next Generation Sequencing (NGS)
Laboratory:
Centre de Génétique-Institut de Pathologie et de Génétique (IPG)
RIZIV code:
565456-565460
Turnaround time (maximum):
20 - 60 days
Document(s):
Created:
06 Aug 2019 - 08:56
Changed:
25 Mar 2022 - 08:04