F13B Sequencing

Mutations in F13B result in factor XIIIB deficiency, which is characterized by increased bleeding and poor wound healing. This condition is inherited in an autosomal recessive manner. This laboratory performs Sanger sequencing of the F13B gene.

Forms & Docs

Ordering

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Test Code
S0961

Turn Around Time
3-5 weeks

Billing

CPT Code
81479×1

Ordering Guidance

If there are questions regarding this test, please contact Client Services at 617-553-5880 or clientservices@claritasgenomics.com

Details

Genes Covered
F13B

Methods
Sanger