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Test Code 10625

Congenital Disorders of Glycosylation (CDG) Panel

54 genes

2 - 3 weeks (7 - 16 days STAT)

Who is this test for?
  • Individuals with relevant features who have a clinical or suspected diagnosis of a Congenital Disorder of Glycosylation (CDG)
  • Individuals with abnormal serum transferrin isoform results
  • Individuals with abnormal glycosylation results on cellular biomarkers
Method
NGS with CNV (Exome or Genome Platform)
Specimen(s)

Exome Platform: Blood, DNA, Buccal, Saliva, Tissue

Genome Platform: Blood, DNA

Order Options

Platform
Test type
OTHER OPTIONS
for pricing.

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