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CPT2 - Carnitine Palmitoyltransferase deficiency type II

This product is also part of the following panels:

Comprehensive preconception carrier test panel¹
Epilepsy panel
Heart disorders panel¹
Mendelian inherited disorders panel with genome wide CNV analysis
Metabolic disorders panel
Muscle disorders panel

OMIM: 600650
Performing laboratory: Radboudumc
Authorized material(s): EDTA blood, Isolated DNA, Buccal mucous membrane

GEN

complete analysis

targeted analysis of a familial mutation

€ 725

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