CLDN19 - hypomagnesemia, autosomal recessive

This test is available for the following conditions:

  • Conditions > Renal / Nephrological > Hypomagnesemia, renal

This product is also part of the following panels:

  • Comprehensive preconception carrier test panel¹
  • Epilepsy panel
  • Mendelian inherited disorders panel with genome wide CNV analysis
  • 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: 610036
Performing laboratory: Radboudumc
Authorized material(s): EDTA blood, Isolated DNA, Buccal mucous membrane




€ 345

Gene

CLDN16 - hypomagnesemia, autosomal recessive

Turnaround time
Complete analysis: 8 weeks / Targeted analysis: 4 weeks
Performing laboratory
Radboudumc
€ 353

CLDN16 - hypomagnesemia, autosomal recessive



€ 353

CLDN16 - hypomagnesemia, autosomal recessive

This test is available for the following conditions:

  • Conditions > Renal / Nephrological > Hypomagnesemia, renal

This product is also part of the following panels:

  • Comprehensive preconception carrier test panel¹
  • Epilepsy panel
  • Mendelian inherited disorders panel with genome wide CNV analysis
  • Renal 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: 603959
Performing laboratory: Radboudumc
Authorized material(s): EDTA blood, Isolated DNA, Buccal mucous membrane




€ 353
Gene

CLDN19 - hypomagnesemia, autosomal recessive

Turnaround time
Complete analysis: 8 weeks / Targeted analysis: 4 weeks
Performing laboratory
Radboudumc
€ 345

CLDN19 - hypomagnesemia, autosomal recessive



€ 345
Gene

CNNM2 - autosomal dominant hypomagnesemia

Turnaround time
Complete analysis: 8 weeks / Targeted analysis: 4 weeks
Performing laboratory
Radboudumc
€ 402

CNNM2 - autosomal dominant hypomagnesemia



€ 402

CNNM2 - autosomal dominant hypomagnesemia

This test is available for the following conditions:

  • Conditions > Renal / Nephrological > Hypomagnesemia, renal

This product is also part of the following panels:

  • Comprehensive preconception carrier test panel¹
  • Epilepsy panel
  • Intellectual disability panel with genome wide CNV analysis
  • Mendelian inherited disorders panel with genome wide CNV analysis
  • Renal 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: 607803
Performing laboratory: Radboudumc
Authorized material(s): EDTA blood, Isolated DNA, Buccal mucous membrane




€ 402
Gene

EGF - autosomal recessive hypomagnesemia

Turnaround time
Complete analysis: 8 weeks / Targeted analysis: 4 weeks
Performing laboratory
Radboudumc
€ 509

EGF - autosomal recessive hypomagnesemia



€ 509

EGF - autosomal recessive hypomagnesemia

This test is available for the following conditions:

  • Conditions > Renal / Nephrological > Hypomagnesemia, renal

This product is also part of the following panels:

  • Comprehensive preconception carrier test panel¹
  • Epilepsy panel
  • Mendelian inherited disorders panel with genome wide CNV analysis
  • Renal 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: 131530
Performing laboratory: Radboudumc
Authorized material(s): EDTA blood, Isolated DNA, Buccal mucous membrane




€ 509
Gene

FXYD2 - autosomal dominant hypomagnesemia

Turnaround time
Complete analysis: 8 weeks / Targeted analysis: 4 weeks
Performing laboratory
Radboudumc
€ 344

FXYD2 - autosomal dominant hypomagnesemia



€ 344

FXYD2 - autosomal dominant hypomagnesemia

This test is available for the following conditions:

  • Conditions > Renal / Nephrological > Hypomagnesemia, renal

This product is also part of the following panels:

  • Epilepsy panel
  • Mendelian inherited disorders panel with genome wide CNV analysis
  • Renal 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: 601814
Performing laboratory: Radboudumc
Authorized material(s): EDTA blood, Isolated DNA, Buccal mucous membrane




€ 344
Gene

KCNA1 - hypomagnesemia with myokymia

Turnaround time
Complete analysis: 8 weeks / Targeted analysis: 4 weeks
Performing laboratory
Radboudumc
€ 345

KCNA1 - hypomagnesemia with myokymia



€ 345

KCNA1 - hypomagnesemia with myokymia

This test is available for the following conditions:

  • Conditions > Renal / Nephrological > Hypomagnesemia, renal

This product is also part of the following panels:

  • Epilepsy panel
  • Mendelian inherited disorders panel with genome wide CNV analysis
  • Movement 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: 176260
Performing laboratory: Radboudumc
Authorized material(s): EDTA blood, Isolated DNA, Buccal mucous membrane




€ 345