Facioscapulohumeral Muscular Dystrophy 2 (hypomethylation D4Z4 repeats)
Full name: |
Facioscapulohumeral Muscular Dystrophy 2 (hypomethylation D4Z4 repeats)
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Test type: |
Clinical
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Test specialty: |
Molecular Genetics
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Test purpose: |
Post-natal Diagnosis
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Specimen: |
Peripheral (whole) blood on EDTA
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Method category: | |
Method technique: | |
Laboratory: | |
RIZIV code: | |
Turnaround time (maximum): |
20 - 60 days
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Document(s): | |
Created: |
01 Aug 2018 - 11:55
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Changed: |
19 Apr 2022 - 12:18
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