GBE1 - adult form of polyglucosan body disease
This test is available for the following conditions:
- Conditions > Neuromuscular > Polyglucosan body disease, adult form
This product is also part of the following panels:
- WES comprehensive preconception carrier test ¹
- WES fetal akinesia (% *)
- WES heart disorders¹ (% *)
- WES liver disorders (% *)
- WES Mendelian inherited disorders (% *)
- WES metabolic disorders (% *)
- WES movement disorders (% *)
- WES muscle disorders (% *)
- WES neuropathies¹ (% *)
* % 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:
607839
Performing laboratory: Radboudumc
Authorized material(s): EDTA blood, Isolated DNA, Buccal mucous membrane