ALS2 - infantile-onset ascending hereditary spastic paralysis

This test is available for the following conditions:

  • Conditions > Neurological > Spastic paralysis, infantile onset ascending (IAHSP)

This product is also part of the following panels:

  • WES amyotrophic lateral sclerosis, ALS (100.0% *)
  • WES comprehensive preconception carrier test ¹
  • WES Mendelian inherited disorders (100.0% *)
  • WES movement disorders (100.0% *)

* % 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: 606352
Performing laboratory: Radboudumc
Authorized material(s): EDTA blood, Isolated DNA, Buccal mucous membrane




€ 583

Gene

ALS2 - infantile-onset ascending hereditary spastic paralysis

Turnaround time
Complete analysis: 8 weeks / Targeted analysis: 4 weeks
Performing laboratory
Radboudumc
€ 583

ALS2 - infantile-onset ascending hereditary spastic paralysis



€ 583