Tyrosine hydroxylase deficiency

TH - tyrosine hydroxylase deficiency

This test is available for the following conditions:

• Conditions > Iron disorders > Tyrosine hydroxylase deficiency

This product is also part of the following panels:

• WES comprehensive preconception carrier test ¹
• WES intellectual disability (100.0% *)
• WES Mendelian inherited disorders (100.0% *)
• WES metabolic disorders (100.0% *)
• WES movement disorders (100.0% *)
• WES Parkinson disease (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: 191290
Performing laboratory: Radboudumc
Authorized material(s): EDTA blood, Isolated DNA, Buccal mucous membrane

---