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ATP1A3 - CAPOS syndrome

This test is available for the following conditions:

Conditions > Neurological > CAPOS syndrome
Conditions > Vision impairment / blindness > CAPOS syndrome

This product is also part of the following panels:

Epilepsy panel
Hearing impairment panel (including GJB2)
Intellectual disability panel with genome wide CNV analysis
Mendelian inherited disorders panel with genome wide CNV analysis
Movement disorders panel
Parkinson disease panel

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

Method

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

OMIM: 601338
Performing laboratory: Radboudumc
Authorized material(s): EDTA blood, Isolated DNA, Buccal mucous membrane

GEN

complete analysis

targeted analysis of a familial mutation

€ 460

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CAPOS syndrome

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Gene

ATP1A3 - CAPOS syndrome

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

Performing laboratory
Radboudumc

€ 460

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ATP1A3 - CAPOS syndrome

GEN

complete analysis

targeted analysis of a familial mutation

€ 460

Add Update Remove

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