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CFHR4 - complement-mediated kidney disease

This test is available for the following conditions:

Conditions > Metabolic disorders > Biotinidase deficiency

This product is also part of the following panels:

Age-related macular degeneration panel
Complement mediated renal disease panel
Mendelian inherited disorders panel with genome wide CNV analysis

Turnaround time
Complete analysis: 8 weeks / Targeted analysis: 4 weeks

Method

Sequence analysis of all coding exons and flanking intron-exon boundaries

OMIM: 605337
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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- Radboudumc & MaasrichtUMC+

Biotinidase deficiency

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Gene

CFHR4 - complement-mediated kidney disease

Turnaround time
Complete analysis: 8 weeks / Targeted analysis: 4 weeks

Performing laboratory
Radboudumc

€ 725

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CFHR4 - complement-mediated kidney disease

GEN

complete analysis

targeted analysis of a familial mutation

€ 725

Add Update Remove

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