Gene

ANO10 - autosomal recessive cerebellar ataxia

Turnaround time
Complete analysis: 8 weeks / Targeted analysis: 4 weeks
Performing laboratory
Radboudumc
€ 699

ANO10 - autosomal recessive cerebellar ataxia



€ 699

ANO10 - autosomal recessive cerebellar ataxia

This test is available for the following conditions:

  • Conditions > Neurological > Spinocerebellar ataxia, autosomal recessive

This product is also part of the following panels:

** % of the coding region of this gene has a coverage of >20x. (Without % information : This is a non-coding gene for which coverage statistics could not be determined)

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

Method

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

OMIM: 613726
Performing laboratory: Radboudumc
Authorized material(s): EDTA blood, Isolated DNA, Buccal mucous membrane




€ 699
Gene

CLN3 - neuronal ceroid lipofuscinosis type 3

Turnaround time
Complete analysis: 8 weeks / Targeted analysis: 4 weeks
Performing laboratory
Radboudumc
€ 687

CLN3 - neuronal ceroid lipofuscinosis type 3



€ 687

CLN3 - neuronal ceroid lipofuscinosis type 3

This test is available for the following conditions:

  • Conditions > Neurological > Spinocerebellar ataxia, autosomal recessive

This product is also part of the following panels:

** % of the coding region of this gene has a coverage of >20x. (Without % information : This is a non-coding gene for which coverage statistics could not be determined)

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

Method

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

OMIM: 204200
Performing laboratory: Radboudumc
Authorized material(s): EDTA blood, Isolated DNA, Buccal mucous membrane




€ 687
Gene

CLN5 - neuronal ceroid lipofuscinosis type 5

Turnaround time
Complete analysis: 8 weeks / Targeted analysis: 4 weeks
Performing laboratory
Radboudumc
€ 969

CLN5 - neuronal ceroid lipofuscinosis type 5



€ 969

CLN5 - neuronal ceroid lipofuscinosis type 5

This test is available for the following conditions:

  • Conditions > Neurological > Spinocerebellar ataxia, autosomal recessive

This product is also part of the following panels:

** % of the coding region of this gene has a coverage of >20x. (Without % information : This is a non-coding gene for which coverage statistics could not be determined)

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

Method

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

OMIM: 608102
Performing laboratory: Radboudumc
Authorized material(s): EDTA blood, Isolated DNA, Buccal mucous membrane




€ 969
Gene

COQ8A (ADCK3) - autosomal recessive spinocerebellar ataxia type 9 (SCA9)

Turnaround time
Complete analysis: 8 weeks / Targeted analysis: 4 weeks
Performing laboratory
Radboudumc
€ 665

COQ8A (ADCK3) - autosomal recessive spinocerebellar ataxia type 9 (SCA9)



€ 665

COQ8A (ADCK3) - autosomal recessive spinocerebellar ataxia type 9 (SCA9)

This test is available for the following conditions:

  • Conditions > Neurological > Spinocerebellar ataxia, autosomal recessive

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

Method

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

OMIM: 606980
Performing laboratory: Radboudumc
Authorized material(s): EDTA blood, Isolated DNA, Buccal mucous membrane




€ 665
Gene

SETX - autosomal recessive spinocerebellar ataxia type 1

Turnaround time
Complete analysis: 8 weeks / Targeted analysis: 4 weeks
Performing laboratory
Radboudumc
€ 1305

SETX - autosomal recessive spinocerebellar ataxia type 1



€ 1305

SETX - autosomal recessive spinocerebellar ataxia type 1

This test is available for the following conditions:

  • Conditions > Neurological > Spinocerebellar ataxia, autosomal recessive

This product is also part of the following panels:

** % of the coding region of this gene has a coverage of >20x. (Without % information : This is a non-coding gene for which coverage statistics could not be determined)

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

Method

  • Sequence analysis of all coding exons and flanking intron-exon boundaries
  • Deletion/duplication analysis (MLPA)

OMIM: 608465
Performing laboratory: Radboudumc
Authorized material(s): EDTA blood, Isolated DNA, Buccal mucous membrane




€ 1305
Gene

TDP1 - autosomal recessive spinocerebellar ataxia with axonal neuropathy

Turnaround time
Complete analysis: 8 weeks / Targeted analysis: 4 weeks
Performing laboratory
Radboudumc
€ 733

TDP1 - autosomal recessive spinocerebellar ataxia with axonal neuropathy



€ 733

TDP1 - autosomal recessive spinocerebellar ataxia with axonal neuropathy

This test is available for the following conditions:

  • Conditions > Neurological > Spinocerebellar ataxia, autosomal recessive

This product is also part of the following panels:

** % of the coding region of this gene has a coverage of >20x. (Without % information : This is a non-coding gene for which coverage statistics could not be determined)

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

Method

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

OMIM: 607198
Performing laboratory: Radboudumc
Authorized material(s): EDTA blood, Isolated DNA, Buccal mucous membrane




€ 733
Gene

WWOX - autosomal recessive cerebellar ataxia with epilepsy and intellectual disability

Turnaround time
Complete analysis: 8 weeks / Targeted analysis: 4 weeks
Performing laboratory
Radboudumc
€ 642

WWOX - autosomal recessive cerebellar ataxia with epilepsy and intellectual disability



€ 642

WWOX - autosomal recessive cerebellar ataxia with epilepsy and intellectual disability

This test is available for the following conditions:

  • Conditions > Neurological > Spinocerebellar ataxia, autosomal recessive

This product is also part of the following panels:

** % of the coding region of this gene has a coverage of >20x. (Without % information : This is a non-coding gene for which coverage statistics could not be determined)

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

Method

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

OMIM: 605131
Performing laboratory: Radboudumc
Authorized material(s): EDTA blood, Isolated DNA, Buccal mucous membrane




€ 642