SQSTM1 - Paget disease of bone 3 ¹

This test is available for the following conditions:

  • Conditions > Multiple congenital anomalies (MCA) > Paget disease of bone 3

This product is also part of the following panels:

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

* % 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: 601530
Performing laboratory: Maastricht UMC+
Authorized material(s): EDTA blood, Isolated DNA, Buccal mucous membrane




€ 378

Gene

SQSTM1 - Paget disease of bone 3 ¹

Turnaround time
Complete analysis: 8 weeks / Targeted analysis: 4 weeks
Performing laboratory
Maastricht UMC+
€ 378

SQSTM1 - Paget disease of bone 3 ¹



€ 378