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POLG2 - Progressive external ophthalmoplegia with mitochondrial DNA deletions

This product is also part of the following panels:

Mendelian inherited disorders panel with genome wide CNV analysis
Mitochondrial disorders panel
Muscle disorders panel
Polyneuropathies panel¹
Vision disorders panel

OMIM: 604983
Performing laboratory: Radboudumc
Authorized material(s): EDTA blood, Isolated DNA, Buccal mucous membrane

GEN

complete analysis

targeted analysis of a familial mutation

€ 761

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