Parkinson (gene panel)
This test requires filling out a specific Application Form available in the "document" field
Full name: |
Parkinson (gene panel)
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Description: |
Content of the panel 6 core genes: PRKN (NM_004562.2, PARK2, parkin), LRRK2 (NM_198578.3, PARK8), DJ-1 (NM_007262.4, PARK7), SNCA (NM_000345.3, PARK4), PINK1 (NM_032409.2, PARK6) andVPS35 (NM_018206.5, PARK17). 10 genes that may be associated with an inherited form of disease of Parkinson: ATP13A2 (NM_022089.3), ATP1A3 (NM_152296.5), ATP6AP2 (NM_005765.2), CHCHD2 (NM_016139.3), DNAJC13 (NM_015268.3), DNAJC6 (NM_001256864.1), FBXO7 (NM_012179.3), PLA2G6 (NM_003560.3), RAB39B (NM_171998.3) and SYNJ1 (NM_003895.3) 2 risk factor genes: GBA gene (NM_001005741.2) and GCH1 gene (NM_000161.2) |
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): |
6 - 9 months
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Document(s): |
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Created: |
22 Jul 2019 - 14:38
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Changed: |
23 Sep 2022 - 11:27
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URL: |