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OCRL - Lowe oculocerebrorenal syndrome

This test is available for the following conditions:

Conditions > Renal / Nephrological > Lowe oculocerebrorenal syndrome

This product is also part of the following panels:

Ciliopathies panel
Hemostatic/thrombotic disorders panel
Intellectual disability panel with genome wide CNV analysis
Mendelian inherited disorders panel with genome wide CNV analysis
Metabolic disorders panel
Renal disorders panel
Vision disorders panel

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

Method

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

OMIM: 300535
Performing laboratory: Radboudumc
Authorized material(s): EDTA blood, Isolated DNA, Buccal mucous membrane

GEN

complete analysis

targeted analysis of a familial mutation

€ 492

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Lowe oculocerebrorenal syndrome

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Gene

OCRL - Lowe oculocerebrorenal syndrome

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

Performing laboratory
Radboudumc

€ 492

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OCRL - Lowe oculocerebrorenal syndrome

GEN

complete analysis

targeted analysis of a familial mutation

€ 492

Add Update Remove

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