Lynch syndrome - MLH1 promoter hypermethylation and BRAF V600E mutation
Full name: |
Lynch syndrome - MLH1 promoter hypermethylation and BRAF V600E mutation
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Description: |
MLH1 promoter gene hypermethylation and screening for V600E BRAF mutation |
Test type: |
Clinical
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Test specialty: |
Molecular Genetics
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Test purpose: |
Carrier diagnosis,
Therapeutic Management
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Specimen: |
Paraffine block of tumor
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Method category: | |
Method technique: | |
Laboratory: | |
RIZIV code: | |
EQA: |
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Accreditation (ISO 15189): |
2022-02-24 / 2026-02-23
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Turnaround time (maximum): |
2 months
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Document(s): | |
Created: |
24 Dec 2019 - 07:59
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Changed: |
23 Jan 2023 - 13:12
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URL: |