GLA - Fabry disease ¹
This test is available for the following conditions:
- Conditions > Cardiovascular > Fabry disease
This product is also part of the following panels:
- WES hearing impairment (including GJB2) (% *)
- WES heart disorders¹ (% *)
- WES hypertrophic cardiomyopathy ¹ (% *)
- WES Mendelian inherited disorders (% *)
- WES metabolic disorders (% *)
- WES neurological pain disorders¹ (% *)
- WES neuropathies¹ (% *)
- WES painful peripheral neuropathies¹ (% *)
- WES renal disorders (% *)
- WES skin disorders¹ (% *)
* % 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 & Targeted analysis: 4 weeks
Method
- Sequence analysis of all coding exons and flanking intron-exon boundaries
OMIM:
300644
Performing laboratory: Radboudumc & Maastricht UMC+
Authorized material(s): EDTA blood, Isolated DNA, Buccal mucous membrane