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OPA3 - Optic atrophy

This product is also part of the following panels:

Comprehensive preconception carrier test panel¹
Hereditary optic neuropathies panel
Intellectual disability / developmental delay panel with genome wide CNV analysis
Mendelian inherited disorders panel with genome wide CNV analysis
Metabolic disorders panel
Mitochondrial disorders panel
Vision disorders panel

OMIM: 606580
Performing laboratory: Radboudumc & Maastricht UMC+
Authorized material(s): EDTA blood, Isolated DNA, Buccal mucous membrane

GEN

complete analysis

targeted analysis of a familial mutation

€ 725

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- Radboudumc & MaasrichtUMC+

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